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Q57394328-1F2E2A66-B6E7-4962-B790-0E1A76975539
Q57394328-1F2E2A66-B6E7-4962-B790-0E1A76975539
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57394328-1F2E2A66-B6E7-4962-B790-0E1A76975539
Congenital Muscular Dystrophy Associated With Merosin Deficiency
P2860
Q57394328-1F2E2A66-B6E7-4962-B790-0E1A76975539
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57394328-1F2E2A66-B6E7-4962-B790-0E1A76975539
rank
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type
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Statement
wasDerivedFrom
eaa63d96818abe87dde01f070817192f58e2b061
P2860
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity