Molecular diagnosis of axonal forms of Charcot-Marie-Tooth disease;Diagnostic moléculaire des formes axonales de la maladie de Charcot-Marie-Tooth

Revue Neurologique

Volumn 165, Issue 12, 2009, Pages 1122-1126

  Latour, P ^a,b   Vial, C ^a,c  

^a Centre de référence maladies neuromusculaires rares Rhône Alpes   (France)

^b HOSPICES CIVILS DE LYON   (France)

^c HÔPITAL NEUROLOGIQUE   (France)

Author keywords

Charcot Marie Tooth; CMT2; Molecular diagnosis strategy

Indexed keywords

CONNEXIN 32; HEAT SHOCK PROTEIN; LAMIN A; LAMIN C; MITOFUSIN 2;

CONTROLLED STUDY; DIAGNOSTIC PROCEDURE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; INHERITANCE; MAJOR CLINICAL STUDY; MOTOR NERVE CONDUCTION; REVIEW;

AXONS; CHARCOT-MARIE-TOOTH DISEASE; DNA, MITOCHONDRIAL; HUMANS; MELAS SYNDROME; MERRF SYNDROME; MITOCHONDRIAL DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES;

EID: 71549135518     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neurol.2009.10.002     Document Type: Review

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