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Q36406976-FC5DDD81-B026-4D3A-9A5E-84D9ECB8D306
Q36406976-FC5DDD81-B026-4D3A-9A5E-84D9ECB8D306
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Statement
http://www.wikidata.org/entity/statement/Q36406976-FC5DDD81-B026-4D3A-9A5E-84D9ECB8D306
Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathy.
P2860
Q36406976-FC5DDD81-B026-4D3A-9A5E-84D9ECB8D306
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36406976-FC5DDD81-B026-4D3A-9A5E-84D9ECB8D306
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wasDerivedFrom
9a744e674ef4e1644b4ec7fe666ef2e8ca4b834c
P2860
Intravenous immune globulin in hereditary inclusion body myopathy: a pilot study