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Q41823092-F4B96E8C-DD37-408D-9C3D-42994CC6ED0A
Q41823092-F4B96E8C-DD37-408D-9C3D-42994CC6ED0A
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Statement
http://www.wikidata.org/entity/statement/Q41823092-F4B96E8C-DD37-408D-9C3D-42994CC6ED0A
A common disease-associated missense mutation in alpha-sarcoglycan fails to cause muscular dystrophy in mice.
P2860
Q41823092-F4B96E8C-DD37-408D-9C3D-42994CC6ED0A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41823092-F4B96E8C-DD37-408D-9C3D-42994CC6ED0A
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wasDerivedFrom
f8455ff700e93a76a567cfb8693c5f9c034791a8
P2860
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity