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Q47686004-E99085C9-854C-49BF-B290-669601487E0C
Q47686004-E99085C9-854C-49BF-B290-669601487E0C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47686004-E99085C9-854C-49BF-B290-669601487E0C
Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies.
P2860
Q47686004-E99085C9-854C-49BF-B290-669601487E0C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47686004-E99085C9-854C-49BF-B290-669601487E0C
rank
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type
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Statement
wasDerivedFrom
3e57724bb8b7629acbc6e9958aae22db621d3504
P2860
CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis.