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Q33547163-E938A33C-0DAB-43C2-8917-687B17B19E48
Q33547163-E938A33C-0DAB-43C2-8917-687B17B19E48
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33547163-E938A33C-0DAB-43C2-8917-687B17B19E48
MFN2 point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families.
P2860
Q33547163-E938A33C-0DAB-43C2-8917-687B17B19E48
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33547163-E938A33C-0DAB-43C2-8917-687B17B19E48
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wasDerivedFrom
d89e4edcb45891c5fb94ffe63188aff0d31be4db
P2860
Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.