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Q42108667-C0AED7F3-A2F2-48C8-8EC3-EF5E9C8AC399
Q42108667-C0AED7F3-A2F2-48C8-8EC3-EF5E9C8AC399
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http://www.wikidata.org/entity/statement/Q42108667-C0AED7F3-A2F2-48C8-8EC3-EF5E9C8AC399
Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codon.
P2860
Q42108667-C0AED7F3-A2F2-48C8-8EC3-EF5E9C8AC399
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42108667-C0AED7F3-A2F2-48C8-8EC3-EF5E9C8AC399
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wasDerivedFrom
f02eb565d9ca575b3a96f9d15526dc4d7ec9b990
P2860
Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N gene.