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Q28296180-A610DFBB-5A8F-4356-AF76-BCB8DF390DAA
Q28296180-A610DFBB-5A8F-4356-AF76-BCB8DF390DAA
BestRank
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http://www.wikidata.org/entity/statement/Q28296180-A610DFBB-5A8F-4356-AF76-BCB8DF390DAA
Structure of the human laminin alpha2-chain gene (LAMA2), which is affected in congenital muscular dystrophy
P2860
Q28296180-A610DFBB-5A8F-4356-AF76-BCB8DF390DAA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28296180-A610DFBB-5A8F-4356-AF76-BCB8DF390DAA
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wasDerivedFrom
b929ed759f65237cb8e675e33f8d98189cc4c45c
P2860
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity