Sensorineural deafness in X-linked Charcot-Marie-Tooth disease with connexin 32 mutation (R142Q)

Neurology

Volumn 52, Issue 5, 1999, Pages 1010-1014

  Stojkovic, Tanya ^b   Latour, P ^a   Vandenberghe, A ^a   Hurtevent, J F ^c   Vermersch, P ^c  

^a Clinical Psychology Unit   (France)

^b LILLE UNIVERSITY HOSPITAL   (France)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 32;

ADULT; AMINO ACID SUBSTITUTION; AREFLEXIA; ARTICLE; CHILD; CLINICAL ARTICLE; CODON; FAMILY HISTORY; FEMALE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MISSENSE MUTATION; MOTOR NERVE CONDUCTION; PEDIGREE ANALYSIS; PERCEPTION DEAFNESS; PHENOTYPE; PRIORITY JOURNAL; SENSORY NERVE CONDUCTION; VIBRATION SENSE; X CHROMOSOME LINKAGE;

EID: 0033596845     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.52.5.1010     Document Type: Article

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