Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome.
Toydemir RM; Rutherford A; Whitby FG; Jorde LB; Carey JC; Bamshad MJ; Nature Genetics, 2006, vol. 38, issue 5, p 561, ISSN 10614036. ISBN 10614036.

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