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Q38552890-559A40B4-7E01-432F-BB76-B1312163CCD6
Q38552890-559A40B4-7E01-432F-BB76-B1312163CCD6
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Statement
http://www.wikidata.org/entity/statement/Q38552890-559A40B4-7E01-432F-BB76-B1312163CCD6
Mitochondrial abnormalities in the myofibrillar myopathies.
P2860
Q38552890-559A40B4-7E01-432F-BB76-B1312163CCD6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38552890-559A40B4-7E01-432F-BB76-B1312163CCD6
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wasDerivedFrom
db0f59ecc0136fa487413f0428955d8428312a07
P2860
A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A).