Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion

Neurology

Volumn 52, Issue 7, 1999, Pages 1440-1446

  Mouton, P ^a   Tardieu, S ^b   Gouider, R ^a   Birouk, N ^a   Maisonobe, T ^a   Dubourg, O ^a   Brice, A ^b   LeGuern, E ^b   Bouche, Pierre ^a,c  

^a AP HP   (France)

^b INSERM   (France)

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CHROMOSOME 17P; CLINICAL FEATURE; DNA DETERMINATION; ELECTROPHYSIOLOGY; FEMALE; GENE DELETION; GENETIC ANALYSIS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MAJOR CLINICAL STUDY; MALE; MOTONEURON; NERVE CONDUCTION; PARALYSIS; POINT MUTATION; PRIORITY JOURNAL;

EID: 0033594507     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.52.7.1440     Document Type: Article

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