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Q49963380-0A136899-481C-4628-88B8-4335C0EF8E57
Q49963380-0A136899-481C-4628-88B8-4335C0EF8E57
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49963380-0A136899-481C-4628-88B8-4335C0EF8E57
A Homozygous LAMA2 Mutation of c.818G>A Caused Partial Merosin Deficiency in a Japanese patient.
P932
Q49963380-0A136899-481C-4628-88B8-4335C0EF8E57
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49963380-0A136899-481C-4628-88B8-4335C0EF8E57
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
162cf43d3678ef7d7bec563d3c2425afca596143
P932
5891531
http://www.w3.org/2001/XMLSchema#string