Associated Papers
A human de novo mutation in MYH10 phenocopies the loss of function mutation in mice.
Tuzovic L et al.
Rare Diseases (austin, Tex.), 2013
25003005 (PubMed )
Supplement: rdis-1-e26144-s01.pdf
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Tuzovic L et al.
Rare Diseases (austin, Tex.), 2013