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Q24633171-91DD7265-69B7-49BE-B080-74159E72FC28
Q24633171-91DD7265-69B7-49BE-B080-74159E72FC28
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24633171-91DD7265-69B7-49BE-B080-74159E72FC28
Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathies
P2860
Q24633171-91DD7265-69B7-49BE-B080-74159E72FC28
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24633171-91DD7265-69B7-49BE-B080-74159E72FC28
rank
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type
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Statement
wasDerivedFrom
051ad7f7535399dee729abe8d830cf89b0210a91
P2860
Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.