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Q49963380-5DB3AC22-B251-4783-A777-A70C5C0EA83B
Q49963380-5DB3AC22-B251-4783-A777-A70C5C0EA83B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49963380-5DB3AC22-B251-4783-A777-A70C5C0EA83B
A Homozygous LAMA2 Mutation of c.818G>A Caused Partial Merosin Deficiency in a Japanese patient.
P2860
Q49963380-5DB3AC22-B251-4783-A777-A70C5C0EA83B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49963380-5DB3AC22-B251-4783-A777-A70C5C0EA83B
rank
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type
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wasDerivedFrom
fc8c949d5d184e48169f22c611c05d003405d6cb
P2860
Laminin-211 in skeletal muscle function.