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Dejerine-Sottas disease with de novo dominant point mutation of the PMP22 gene

Victor Ionâşescu, R. Ionasescu, Ch. Searby, R. Neahring
DOI: 10.1212/wnl.45.9.1766
Neurology

Data up to Jan 2025

Published1995
Citations52
References2
Fields
BiologyMedicineGenetics

Total Citations Per Year

Abstract

References (2)

CLINICAL AND ELECTRODIAGNOSTIC FEATURES OF CHARCOT-MARIE-TOOTH SYNDROME

1978 • 89 citations

Cardiomyopathy revisited

1993 • 20 citations

Cited By (0)

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Dejerine-Sottas disease with de novo dominant point mutation of the PMP22 gene (1995) – Neurology | Metascience Observatory Explorer