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National Institutes of Health
CONE-ROD DYSTROPHY, X-LINKED, 3
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Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients.
I. V. Mersiyanova
S. M. Ismailov
Corpus ID: 46226343
Charcot-Marie-Tooth disease (CMT) and related inherited peripheral neuropathies, including Dejerine-Sottas syndrome, congenital…
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