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Q38089840-01DD5F6C-78DA-4626-A4D3-FCE385DB6C3E
Q38089840-01DD5F6C-78DA-4626-A4D3-FCE385DB6C3E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38089840-01DD5F6C-78DA-4626-A4D3-FCE385DB6C3E
Molecular diagnosis of muscular dystrophies, focused on limb girdle muscular dystrophies.
P2860
Q38089840-01DD5F6C-78DA-4626-A4D3-FCE385DB6C3E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38089840-01DD5F6C-78DA-4626-A4D3-FCE385DB6C3E
rank
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Statement
wasDerivedFrom
e78aecaf8115da091b0036e4166345d2a0ba2360
P2860
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity