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Q24807143-1CFBB5B2-01B9-4E9B-A618-F420760805DE
Q24807143-1CFBB5B2-01B9-4E9B-A618-F420760805DE
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Statement
http://www.wikidata.org/entity/statement/Q24807143-1CFBB5B2-01B9-4E9B-A618-F420760805DE
Clinico-pathogenetic findings and management of chondrodystrophic myotonia (Schwartz-Jampel syndrome): a case report
P2860
Q24807143-1CFBB5B2-01B9-4E9B-A618-F420760805DE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24807143-1CFBB5B2-01B9-4E9B-A618-F420760805DE
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type
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Statement
wasDerivedFrom
bb7ee89fbac5228b86703aeb900e0ff2522c31ed
P2860
Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia