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Q24517965-EEBD9149-D476-4BA5-9F16-1B73137F8D39
Q24517965-EEBD9149-D476-4BA5-9F16-1B73137F8D39
BestRank
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http://www.wikidata.org/entity/statement/Q24517965-EEBD9149-D476-4BA5-9F16-1B73137F8D39
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.
P2860
Q24517965-EEBD9149-D476-4BA5-9F16-1B73137F8D39
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24517965-EEBD9149-D476-4BA5-9F16-1B73137F8D39
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wasDerivedFrom
dfb81448066e62b9061ab5874561fa12e0c2302b
P2860
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity