[cite web | title = Entrez Gene: HCCS holocytochrome c synthase (cytochrome c heme-lyase)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3052| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Wapenaar MC, Bassi MT, Schaefer L, "et al." |title=The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions. |journal=Hum. Mol. Genet. |volume=2 |issue= 7 |pages= 947–52 |year= 1993 |pmid= 8364577 |doi=
*cite journal | author=Schaefer L, Ballabio A, Zoghbi HY |title=Cloning and characterization of a putative human holocytochrome c-type synthetase gene (HCCS) isolated from the critical region for microphthalmia with linear skin defects (MLS). |journal=Genomics |volume=34 |issue= 2 |pages= 166–72 |year= 1997 |pmid= 8661044 |doi= 10.1006/geno.1996.0261
*cite journal | author=Van den Veyver IB, Subramanian S, Zoghbi HY |title=Genomic structure of a human holocytochrome c-type synthetase gene in Xp22.3 and mutation analysis in patients with Rett syndrome. |journal=Am. J. Med. Genet. |volume=78 |issue= 2 |pages= 179–81 |year= 1998 |pmid= 9674913 |doi=
*cite journal | author=Schwarz QP, Cox TC |title=Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome c. |journal=Genomics |volume=79 |issue= 1 |pages= 51–7 |year= 2002 |pmid= 11827457 |doi= 10.1006/geno.2001.6677
*cite journal | author=Prakash SK, Cormier TA, McCall AE, "et al." |title=Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant microphthalmia with linear skin defects (MLS) syndrome. |journal=Hum. Mol. Genet. |volume=11 |issue= 25 |pages= 3237–48 |year= 2003 |pmid= 12444108 |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=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=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=Nakashima-Kamimura N, Asoh S, Ishibashi Y, "et al." |title=MIDAS/GPP34, a nuclear gene product, regulates total mitochondrial mass in response to mitochondrial dysfunction. |journal=J. Cell. Sci. |volume=118 |issue= Pt 22 |pages= 5357–67 |year= 2006 |pmid= 16263763 |doi= 10.1242/jcs.02645
*cite journal | author=Wimplinger I, Morleo M, Rosenberger G, "et al." |title=Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome. |journal=Am. J. Hum. Genet. |volume=79 |issue= 5 |pages= 878–89 |year= 2006 |pmid= 17033964 |doi= 10.1086/508474
*cite journal | author=Wimplinger I, Shaw GM, Kutsche K |title=HCCS loss-of-function missense mutation in a female with bilateral microphthalmia and sclerocornea: a novel gene for severe ocular malformations? |journal=Mol. Vis. |volume=13 |issue= |pages= 1475–82 |year= 2007 |pmid= 17893649 |doi=
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