Charcot-Marie-Tooth type 1a in a child with Long QT syndrome

European Journal of Paediatric Neurology

Volumn 13, Issue 5, 2009, Pages 459-462

  Losito, Luciana ^a   De Rinaldis, Marta ^a   Gennaro, Leonarda ^a   Priori, Silvia G ^c   Bloise, Raffaella ^c   Bassi, Maria Teresa ^a   Bresolin, Nereo ^a,b   Trabacca, Antonio ^a  

^a SCIENTIFIC INSTITUTE   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

^c UNIVERSITY OF PAVIA   (Italy)

Author keywords

Charcot Marie Tooth; Demyelinating sensorimotor neuropathy; Ion channels; Long QT syndrome

Indexed keywords

ARTICLE; CARDIOVASCULAR DISEASE; CASE REPORT; CHILD; DNA DETERMINATION; ELECTRONEUROGRAPHY; FAMILY HISTORY; HEART DEPOLARIZATION; HEART FUNCTION; HEREDITARY MOTOR SENSORY NEUROPATHY; HEREDITARY MOTOR SENSORY NEUROPATHY TYPE 1A; HUMAN; LONG QT SYNDROME; MALE; MOTOR DYSFUNCTION; NEUROLOGIC EXAMINATION; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL; SENSORY DYSFUNCTION;

ADULT; CHARCOT-MARIE-TOOTH DISEASE; CHILD; CHROMOSOME DISORDERS; DNA MUTATIONAL ANALYSIS; ELECTROCARDIOGRAPHY, AMBULATORY; ELECTROPHYSIOLOGY; FEMALE; GENE DUPLICATION; HUMANS; LONG QT SYNDROME; MALE; PEDIGREE; YOUNG ADULT;

EID: 68349119093     PISSN: 10903798     EISSN: 15322130     Source Type: Journal    
DOI: 10.1016/j.ejpn.2008.07.011     Document Type: Article

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