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Q35074642-732A7FA9-2502-43B1-8055-3EB15C8130CD
Q35074642-732A7FA9-2502-43B1-8055-3EB15C8130CD
BestRank
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http://www.wikidata.org/entity/statement/Q35074642-732A7FA9-2502-43B1-8055-3EB15C8130CD
Mutation screening of mitofusin 2 in Charcot-Marie-Tooth disease type 2
P2860
Q35074642-732A7FA9-2502-43B1-8055-3EB15C8130CD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35074642-732A7FA9-2502-43B1-8055-3EB15C8130CD
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wasDerivedFrom
3d5d8ef3f44909b4e72bb3674154edf4ce64d474
P2860
Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.