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CACNA1F, EX18-26DEL

National Institutes of Health

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1 relation

CONE-ROD DYSTROPHY, X-LINKED, 3

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Highly Cited

2000

Highly Cited

2000

Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients.

Irina V. Mersiyanova, Sookhrat M. Ismailov, +7 authors Oleg V. Evgrafov
Human mutation
2000

Charcot-Marie-Tooth disease (CMT) and related inherited peripheral neuropathies, including Dejerine-Sottas syndrome, congenital… Expand

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