[cite web | title = Entrez Gene: ELOVL4 elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6785| accessdate = ] ] PBB_Summary
section_title =
summary_text =
References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Zhang K, Bither PP, Park R, "et al." |title=A dominant Stargardt's macular dystrophy locus maps to chromosome 13q34. |journal=Arch. Ophthalmol. |volume=112 |issue= 6 |pages= 759–64 |year= 1994 |pmid= 8002833 |doi=
*cite journal | author=Stone EM, Nichols BE, Kimura AE, "et al." |title=Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q. |journal=Arch. Ophthalmol. |volume=112 |issue= 6 |pages= 765–72 |year= 1994 |pmid= 8002834 |doi=
*cite journal | author=Edwards AO, Miedziak A, Vrabec T, "et al." |title=Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14. |journal=Am. J. Ophthalmol. |volume=127 |issue= 4 |pages= 426–35 |year= 1999 |pmid= 10218695 |doi=
*cite journal | author=Zhang K, Kniazeva M, Han M, "et al." |title=A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy. |journal=Nat. Genet. |volume=27 |issue= 1 |pages= 89–93 |year= 2001 |pmid= 11138005 |doi= 10.1038/83817
*cite journal | author=Li Y, Marcos I, Borrego S, "et al." |title=Evaluation of the ELOVL4 gene in families with retinitis pigmentosa linked to the RP25 locus. |journal=J. Med. Genet. |volume=38 |issue= 7 |pages= 478–80 |year= 2001 |pmid= 11474659 |doi=
*cite journal | author=Edwards AO, Donoso LA, Ritter R |title=A novel gene for autosomal dominant Stargardt-like macular dystrophy with homology to the SUR4 protein family. |journal=Invest. Ophthalmol. Vis. Sci. |volume=42 |issue= 11 |pages= 2652–63 |year= 2001 |pmid= 11581213 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Rivolta C, Ayyagari R, Sieving PA, "et al." |title=Evaluation of the ELOVL4 gene in patients with autosomal recessive retinitis pigmentosa and Leber congenital amaurosis. |journal=Mol. Vis. |volume=9 |issue= |pages= 49–51 |year= 2003 |pmid= 12592226 |doi=
*cite journal | author=Lagali PS, Liu J, Ambasudhan R, "et al." |title=Evolutionarily conserved ELOVL4 gene expression in the vertebrate retina. |journal=Invest. Ophthalmol. Vis. Sci. |volume=44 |issue= 7 |pages= 2841–50 |year= 2003 |pmid= 12824221 |doi=
*cite journal | author=Vrabec TR, Tantri A, Edwards A, "et al." |title=Autosomal dominant Stargardt-like macular dystrophy: identification of a new family with a mutation in the ELOVL4 gene. |journal=Am. J. Ophthalmol. |volume=136 |issue= 3 |pages= 542–5 |year= 2003 |pmid= 12967813 |doi=
*cite journal | author=Mungall AJ, Palmer SA, Sims SK, "et al." |title=The DNA sequence and analysis of human chromosome 6. |journal=Nature |volume=425 |issue= 6960 |pages= 805–11 |year= 2003 |pmid= 14574404 |doi= 10.1038/nature02055
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Ambasudhan R, Wang X, Jablonski MM, "et al." |title=Atrophic macular degeneration mutations in ELOVL4 result in the intracellular misrouting of the protein. |journal=Genomics |volume=83 |issue= 4 |pages= 615–25 |year= 2004 |pmid= 15028284 |doi= 10.1016/j.ygeno.2003.10.004
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Grayson C, Molday RS |title=Dominant negative mechanism underlies autosomal dominant Stargardt-like macular dystrophy linked to mutations in ELOVL4. |journal=J. Biol. Chem. |volume=280 |issue= 37 |pages= 32521–30 |year= 2005 |pmid= 16036915 |doi= 10.1074/jbc.M503411200
*cite journal | author=Lai Z, Zhang XN, Zhou W, "et al." |title=Evaluation of the ELOVL4 gene in a Chinese family with autosomal dominant STGD3-like macular dystrophy. |journal=J. Cell. Mol. Med. |volume=9 |issue= 4 |pages= 961–5 |year= 2006 |pmid= 16364203 |doi=
*cite journal | author=Hubbard AF, Askew EW, Singh N, "et al." |title=Association of adipose and red blood cell lipids with severity of dominant Stargardt macular dystrophy (STGD3) secondary to an ELOVL4 mutation. |journal=Arch. Ophthalmol. |volume=124 |issue= 2 |pages= 257–63 |year= 2006 |pmid= 16476896 |doi= 10.1001/archopht.124.2.257
*cite journal | author=Seitsonen S, Lemmelä S, Holopainen J, "et al." |title=Analysis of variants in the complement factor H, the elongation of very long chain fatty acids-like 4 and the hemicentin 1 genes of age-related macular degeneration in the Finnish population. |journal=Mol. Vis. |volume=12 |issue= |pages= 796–801 |year= 2006 |pmid= 16885922 |doi=
*cite journal | author=McMahon A, Butovich IA, Mata NL, "et al." |title=Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4. |journal=Mol. Vis. |volume=13 |issue= |pages= 258–72 |year= 2007 |pmid= 17356513 |doi=
PBB_Controls
update_page = yes
require_manual_inspection = no
update_protein_box = yes
update_summary = yes
update_citations = yes
