Hemizygosity for SMCHD1 in Facioscapulohumeral Muscular Dystrophy Type 2: Consequences for 18p Deletion Syndrome

Publisher： John Wiley & Sons Inc

E-ISSN： 1098-1004|36|7|679-683

ISSN： 1059-7794

Source： HUMAN MUTATION, Vol.36, Iss.7, 2015-07, pp. : 679-683

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