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Q39044467-14A1C035-7278-4023-A545-E8844B2491E2
Q39044467-14A1C035-7278-4023-A545-E8844B2491E2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39044467-14A1C035-7278-4023-A545-E8844B2491E2
Comparison of Serum rAAV Serotype-Specific Antibodies in Patients with Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, Inclusion Body Myositis, or GNE Myopathy.
P2860
Q39044467-14A1C035-7278-4023-A545-E8844B2491E2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39044467-14A1C035-7278-4023-A545-E8844B2491E2
rank
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type
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Statement
wasDerivedFrom
d50db459354e625769ab376bafe6128e99c61114
P2860
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy