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Q49963380-fa802b4c-e180-43b7-a645-19b0623f46c1
Q49963380-fa802b4c-e180-43b7-a645-19b0623f46c1
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Statement
http://www.wikidata.org/entity/statement/Q49963380-fa802b4c-e180-43b7-a645-19b0623f46c1
A Homozygous LAMA2 Mutation of c.818G>A Caused Partial Merosin Deficiency in a Japanese patient.
P31
Q49963380-fa802b4c-e180-43b7-a645-19b0623f46c1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49963380-fa802b4c-e180-43b7-a645-19b0623f46c1
rank
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type
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P31
case report