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Q49963380-4E460D8A-0DF8-4337-9321-9F7F6AF3BA97
Q49963380-4E460D8A-0DF8-4337-9321-9F7F6AF3BA97
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49963380-4E460D8A-0DF8-4337-9321-9F7F6AF3BA97
A Homozygous LAMA2 Mutation of c.818G>A Caused Partial Merosin Deficiency in a Japanese patient.
P2860
Q49963380-4E460D8A-0DF8-4337-9321-9F7F6AF3BA97
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49963380-4E460D8A-0DF8-4337-9321-9F7F6AF3BA97
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wasDerivedFrom
3871452e9ade74a085fb993bb77ecd5dbf846ade
P2860
Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutations.