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Q37708904-FDEDADC7-60E8-4768-82A6-F699531219F3
Q37708904-FDEDADC7-60E8-4768-82A6-F699531219F3
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http://www.wikidata.org/entity/statement/Q37708904-FDEDADC7-60E8-4768-82A6-F699531219F3
Targeted next generation sequencing identifies two novel mutations in SEPN1 in rigid spine muscular dystrophy 1.
P2860
Q37708904-FDEDADC7-60E8-4768-82A6-F699531219F3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37708904-FDEDADC7-60E8-4768-82A6-F699531219F3
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wasDerivedFrom
5d7272ecb1a8712eab531d84d85a69c3b5e23be2
P2860
Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N gene.