MYH8: Difference between revisions

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{{Infobox_gene}}
'''Myosin-8''' is a [[protein]] that in humans is encoded by the ''MYH8'' [[gene]].<ref name="pmid2373371">{{cite journal |vauthors=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 |date=Aug 1990 | pmid = 2373371 | pmc = | doi =10.1016/0378-1119(90)90020-R }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: MYH8 myosin, heavy chain 8, skeletal muscle, perinatal| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4626| accessdate = }}</ref>
 
Mutations in MYH8 are associated with [[Trismus pseudocamptodactyly syndrome]].