Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2. (Q42071075)

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Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2.
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    Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2. (English)

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