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Q35882763-829640D0-21E1-4AA0-BE23-CF4E9640EE7E
Q35882763-829640D0-21E1-4AA0-BE23-CF4E9640EE7E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35882763-829640D0-21E1-4AA0-BE23-CF4E9640EE7E
Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the protein.
P2860
Q35882763-829640D0-21E1-4AA0-BE23-CF4E9640EE7E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35882763-829640D0-21E1-4AA0-BE23-CF4E9640EE7E
rank
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type
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Statement
wasDerivedFrom
7a36647974527eb6e75d5bc275cb91e253aafb8e
P2860
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity