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A novel point mutation in the peripheral myelin protein 22 (PMP22) gene associated with Charcot-Marie-Tooth disease type 1A

Data up to Jan 2025

Published1997
Citations22
References10

Total Citations Per Year

Abstract

A novel point mutation in the peripheral myelin protein 22 (PMP22) gene associated with… (1997) – Neurology | Metascience Observatory Explorer