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Q47686004-1527849A-5E1A-445E-8601-3BEA6903E3F2
Q47686004-1527849A-5E1A-445E-8601-3BEA6903E3F2
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Statement
http://www.wikidata.org/entity/statement/Q47686004-1527849A-5E1A-445E-8601-3BEA6903E3F2
Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies.
P2860
Q47686004-1527849A-5E1A-445E-8601-3BEA6903E3F2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47686004-1527849A-5E1A-445E-8601-3BEA6903E3F2
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wasDerivedFrom
3e57724bb8b7629acbc6e9958aae22db621d3504
P2860
The allelic spectrum of Charcot-Marie-Tooth disease in over 17,000 individuals with neuropathy.