Patients homozygous for the 17p11.2 Duplication in charcot-marie-tooth type 1a disease

Annals of Neurology

Volumn 41, Issue 1, 1997, Pages 104-108

  LeGuern, E ^a   Gouider, R ^a,c   Mabin, D ^b   Tardieu, S ^a   Birouk, N ^a   Parent, P ^c   Bouche, P ^a   Brice, A ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b BREST UNIVERSITY HOSPITAL   (France)

^c Institut National de Neurologie Tunisia   (Tunisia)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 17P; CLINICAL ARTICLE; DISEASE SEVERITY; FAMILY STUDY; GENETIC LINKAGE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; PERIPHERAL NEUROPATHY; PHENOTYPE; PRIORITY JOURNAL;

ADULT; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; HUMANS; MALE; MIDDLE AGED; MULTIGENE FAMILY; NEURAL CONDUCTION; PEDIGREE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;

EID: 0031031995     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410410117     Document Type: Article

References (21)

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