MYH8

MYH8

Myosin, heavy chain 8, skeletal muscle, perinatal, also known as MYH8, is a human gene.cite web | title = Entrez Gene: MYH8 myosin, heavy chain 8, skeletal muscle, perinatal| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4626| accessdate = ]

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References

Further reading

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*cite journal | author=Bober E, Buchberger-Seidl A, Braun T, "et al." |title=Identification of three developmentally controlled isoforms of human myosin heavy chains. |journal=Eur. J. Biochem. |volume=189 |issue= 1 |pages= 55–65 |year= 1990 |pmid= 1691980 |doi=
*cite journal | author=Bober E, Lyons GE, Braun T, "et al." |title=The muscle regulatory gene, Myf-6, has a biphasic pattern of expression during early mouse development. |journal=J. Cell Biol. |volume=113 |issue= 6 |pages= 1255–65 |year= 1991 |pmid= 2045411 |doi=
*cite journal | author=Karsch-Mizrachi I, Feghali R, Shows TB, Leinwand LA |title=Generation of a full-length human perinatal myosin heavy-chain-encoding cDNA. |journal=Gene |volume=89 |issue= 2 |pages= 289–94 |year= 1990 |pmid= 2373371 |doi=
*cite journal | author=Feghali R, Leinwand LA |title=Molecular genetic characterization of a developmentally regulated human perinatal myosin heavy chain. |journal=J. Cell Biol. |volume=108 |issue= 5 |pages= 1791–7 |year= 1989 |pmid= 2715179 |doi=
*cite journal | author=Jullian EH, Kelly AM, Pompidou AJ, "et al." |title=Characterization of a human perinatal myosin heavy-chain transcript. |journal=Eur. J. Biochem. |volume=230 |issue= 3 |pages= 1001–6 |year= 1995 |pmid= 7601129 |doi=
*cite journal | author=Soussi-Yanicostas N, Whalen RG, Petit C |title=Five skeletal myosin heavy chain genes are organized as a multigene complex in the human genome. |journal=Hum. Mol. Genet. |volume=2 |issue= 5 |pages= 563–9 |year= 1993 |pmid= 8518795 |doi=
*cite journal | author=Veugelers M, Bressan M, McDermott DA, "et al." |title=Mutation of perinatal myosin heavy chain associated with a Carney complex variant. |journal=N. Engl. J. Med. |volume=351 |issue= 5 |pages= 460–9 |year= 2004 |pmid= 15282353 |doi= 10.1056/NEJMoa040584
*cite journal | author=Kimura K, Wakamatsu A, Suzuki Y, "et al." |title=Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. |journal=Genome Res. |volume=16 |issue= 1 |pages= 55–65 |year= 2006 |pmid= 16344560 |doi= 10.1101/gr.4039406
*cite journal | author=Toydemir RM, Chen H, Proud VK, "et al." |title=Trismus-pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8. |journal=Am. J. Med. Genet. A |volume=140 |issue= 22 |pages= 2387–93 |year= 2007 |pmid= 17041932 |doi= 10.1002/ajmg.a.31495

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