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Q34171616-4FAEC0A4-6F04-4F9E-A4F8-CD9397068B4B
Q34171616-4FAEC0A4-6F04-4F9E-A4F8-CD9397068B4B
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Statement
http://www.wikidata.org/entity/statement/Q34171616-4FAEC0A4-6F04-4F9E-A4F8-CD9397068B4B
Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.
P2860
Q34171616-4FAEC0A4-6F04-4F9E-A4F8-CD9397068B4B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34171616-4FAEC0A4-6F04-4F9E-A4F8-CD9397068B4B
rank
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type
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wasDerivedFrom
1a6675c58ca2b93006c178a20ac830966e8f0d84
P2860
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy