A novel GDAP1 mutation 439delA is associated with autosomal recessive CMT disease

Canadian Journal of Neurological Sciences

Volumn 33, Issue 3, 2006, Pages 311-316

  Georgiou, Domna Maria ^a   Nicolaou, Paschalis ^a   Chitayat, David ^b   Koutsou, Pantelitsa ^a   Babul Hirji, Riyana ^b   Vajsar, Jiri ^b   Murphy, Jillian ^b   Christodoulou, Kyproula ^a  

^a CYPRUS INSTITUTE OF NEUROLOGY AND GENETICS   (Cyprus)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

GANGLIOSIDE; GANGLIOSIDE INDUCED DIFFERENTIATION ASSOCIATED PROTEIN 1; UNCLASSIFIED DRUG;

ANAMNESIS; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CHILD; CHROMOSOME 8; CLINICAL FEATURE; CONSANGUINITY; CONTROLLED STUDY; DEMYELINATION; ELECTROPHYSIOLOGY; FEMALE; GENE DELETION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MOLECULAR GENETICS; MOTOR NEUROPATHY; NERVE FIBER; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SENSORY NEUROPATHY; SINGLE NUCLEOTIDE POLYMORPHISM; X CHROMOSOMAL INHERITANCE;

EID: 33748452424     PISSN: 03171671     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0317167100005199     Document Type: Article

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