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Q49963380-7818790F-D6A5-4A0A-83BD-14EE78834644
Q49963380-7818790F-D6A5-4A0A-83BD-14EE78834644
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Statement
http://www.wikidata.org/entity/statement/Q49963380-7818790F-D6A5-4A0A-83BD-14EE78834644
A Homozygous LAMA2 Mutation of c.818G>A Caused Partial Merosin Deficiency in a Japanese patient.
P2860
Q49963380-7818790F-D6A5-4A0A-83BD-14EE78834644
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49963380-7818790F-D6A5-4A0A-83BD-14EE78834644
rank
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wasDerivedFrom
fc8c949d5d184e48169f22c611c05d003405d6cb
P2860
The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review