Molecular and clinical features of inherited neuropathies due to PMP22 duplication

Author:

Watila M.M.,Balarabe S.A.

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference83 articles.

1. Real-time quantitative polymerase chain reaction;Aarskog;Hum. Genet.,2000

2. Roussy–Lévy syndrome is a phenotypic variant of Charcot–Marie–Tooth syndrome IA associated with a duplication on chromosome 17p11.2;Auer-Grumbach;J. Neurol. Sci.,1998

3. Molecular genetics of Charcot–Marie–Tooth disease: from genes to genomes;Azzedine;Mol. Syndromol.,2012

4. Charcot–Marie–Tooth disease: a review with emphasis on the pathophysiology of pes cavus;Berciano;Rev. Esp. Cir. Ortop. Traumatol. (Engl. Ed.),2011

5. Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with Charcot–Marie–Tooth disease 1A duplication;Berciano;Neuromuscul. Disord.,2000

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