Phenotype and clinical evolution of charcot-marie-tooth disease type 1A duplication

Advances in Experimental Medicine and Biology

Volumn 652, Issue , 2009, Pages 183-200

  Berciano, José ^a   García, Antonio ^b   Gallardo, Elena ^b   Ramón, César ^b   Combarros, Onofre ^b  

^a HOSPITAL UNIVERSITARIO MARQUÉS DE VALDECILLA   (Spain)

^b NONE

Author keywords

17p11.2 duplication; Axon; Axonal degeneration; Charcot Marie Tooth disease demyelination; Magnetic resonance imaging; Myelin; Nerve conduction study; Phenotype

Indexed keywords

CLINICAL FEATURE; CONFERENCE PAPER; DISEASE COURSE; GENE DUPLICATION; GENE LOCUS; GENETIC ANALYSIS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; NERVE CONDUCTION; NEUROIMAGING; PATHOPHYSIOLOGY; PHENOTYPE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; GENETICS; LEG; PATHOLOGY; REVIEW;

CHARCOT-MARIE-TOOTH DISEASE; GENE DUPLICATION; HUMANS; LEG; PHENOTYPE;

EID: 77950349652     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-90-481-2813-6_12     Document Type: Conference Paper

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