[cite web | title = Entrez Gene: PLEKHG4 pleckstrin homology domain containing, family G (with RhoGef domain) member 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=25894| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Flanigan K, Gardner K, Alderson K, "et al." |title=Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1. |journal=Am. J. Hum. Genet. |volume=59 |issue= 2 |pages= 392–9 |year= 1996 |pmid= 8755926 |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=Hellenbroich Y, Bubel S, Pawlack H, "et al." |title=Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region. |journal=J. Neurol. |volume=250 |issue= 6 |pages= 668–71 |year= 2003 |pmid= 12796826 |doi= 10.1007/s00415-003-1052-x
*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=Hirano R, Takashima H, Okubo R, "et al." |title=Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families. |journal=Neurogenetics |volume=5 |issue= 4 |pages= 215–21 |year= 2005 |pmid= 15455264 |doi= 10.1007/s10048-004-0194-z
*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=Ishikawa K, Toru S, Tsunemi T, "et al." |title=An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains. |journal=Am. J. Hum. Genet. |volume=77 |issue= 2 |pages= 280–96 |year= 2005 |pmid= 16001362 |doi= 10.1086/432518
*cite journal | author=Wieczorek S, Arning L, Alheite I, Epplen JT |title=Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population. |journal=J. Hum. Genet. |volume=51 |issue= 4 |pages= 363–7 |year= 2006 |pmid= 16491300 |doi= 10.1007/s10038-006-0372-y
*cite journal | author=Lim J, Hao T, Shaw C, "et al." |title=A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration. |journal=Cell |volume=125 |issue= 4 |pages= 801–14 |year= 2006 |pmid= 16713569 |doi= 10.1016/j.cell.2006.03.032
*cite journal | author=Ouyang Y, Sakoe K, Shimazaki H, "et al." |title=16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study. |journal=J. Neurol. Sci. |volume=247 |issue= 2 |pages= 180–6 |year= 2006 |pmid= 16780885 |doi= 10.1016/j.jns.2006.04.009
*cite journal | author=Nozaki H, Ikeuchi T, Kawakami A, "et al." |title=Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population. |journal=Mov. Disord. |volume=22 |issue= 6 |pages= 857–62 |year= 2007 |pmid= 17357132 |doi= 10.1002/mds.21443
*cite journal | author=Amino T, Ishikawa K, Toru S, "et al." |title=Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia. |journal=J. Hum. Genet. |volume=52 |issue= 8 |pages= 643–9 |year= 2007 |pmid= 17611710 |doi= 10.1007/s10038-007-0154-1
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