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Q24632769-26A6AE92-1106-4860-918E-824101645424
Q24632769-26A6AE92-1106-4860-918E-824101645424
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http://www.wikidata.org/entity/statement/Q24632769-26A6AE92-1106-4860-918E-824101645424
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse
P2860
Q24632769-26A6AE92-1106-4860-918E-824101645424
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24632769-26A6AE92-1106-4860-918E-824101645424
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wasDerivedFrom
e0c2db7ee6cb92a08616b5d953839b5f3ef40d0a
P2860
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)