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Q35923554-14B73E24-FD94-4E78-9DF2-10BF452B149B
Q35923554-14B73E24-FD94-4E78-9DF2-10BF452B149B
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http://www.wikidata.org/entity/statement/Q35923554-14B73E24-FD94-4E78-9DF2-10BF452B149B
Laminopathies.
P2860
Q35923554-14B73E24-FD94-4E78-9DF2-10BF452B149B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35923554-14B73E24-FD94-4E78-9DF2-10BF452B149B
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wasDerivedFrom
621aceb002977b4c69092bd869d964baf4fccf95
P2860
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