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Q58134331-F2826D60-2C61-4A5E-B569-25377A251A15
Q58134331-F2826D60-2C61-4A5E-B569-25377A251A15
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http://www.wikidata.org/entity/statement/Q58134331-F2826D60-2C61-4A5E-B569-25377A251A15
Missense mutations ofmitofusin 2in axonal Charcot–Marie–Tooth neuropathy: polymorphic or incomplete penetration?
P2860
Q58134331-F2826D60-2C61-4A5E-B569-25377A251A15
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58134331-F2826D60-2C61-4A5E-B569-25377A251A15
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96f9d0e94a0a9f1ee7616fe996dab772c36ae103
P2860
Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes.