A novel GDAP1 mutation P78L responsible for CMT4A disease in three Moroccan families

Canadian Journal of Neurological Sciences

Volumn 34, Issue 4, 2007, Pages 421-426

  Bouhouche, Ahmed ^a   Birouk, Nazha ^a   Benomar, Ali ^a   Ouazzani, Reda ^a   Chkili, Taïeb ^a   Yahyaoui, Mohamed ^a  

^a IBN SINA HOSPITAL   (Morocco)

Author keywords

[No Author keywords available]

Indexed keywords

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

ADOLESCENT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHARCOT MARIE TOOTH DISEASE TYPE 4A; CLINICAL ARTICLE; CODON; CONTROLLED STUDY; DISEASE DURATION; EXON; FAMILY; FEMALE; GENE MUTATION; GENETIC LINKAGE; GENETIC SCREENING; GENOTYPE; HAPLOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HETEROZYGOTE; HOMOZYGOTE; HUMAN; LIFE; PHENOTYPE; PRIORITY JOURNAL; SYMPTOM; VOICE;

EID: 37049031687     PISSN: 03171671     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0317167100007290     Document Type: Article

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