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Q36012956-05AF7F0D-D4F6-4636-98C3-4AD84D1777CB
Q36012956-05AF7F0D-D4F6-4636-98C3-4AD84D1777CB
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Statement
http://www.wikidata.org/entity/statement/Q36012956-05AF7F0D-D4F6-4636-98C3-4AD84D1777CB
Diagnostic immunohistochemistry in neuromuscular disorders.
P2860
Q36012956-05AF7F0D-D4F6-4636-98C3-4AD84D1777CB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36012956-05AF7F0D-D4F6-4636-98C3-4AD84D1777CB
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wasDerivedFrom
805109f0b4d584e730e3454cb952cdc634f268c2
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