Dejerine-Sottas syndrome and vestibular loss due to a point mutation in the PMP22 gene

Journal of the Neurological Sciences

Volumn 237, Issue 1-2, 2005, Pages 21-24

  Jen, Joanna ^a   Baloh, Robert H ^b   Ishiyama, Akira ^a   Baloh, Robert W ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b MASSACHUSETTS GENERAL HOSPITAL   (United States)

Author keywords

Charcot Marie Tooth; Hearing loss; Imbalance; Oscillopsia

Indexed keywords

PERIPHERAL MYELIN PROTEIN 22;

ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; FAMILY HISTORY; FATHER; FEMALE; GENETIC SCREENING; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MISSENSE MUTATION; NEUROLOGIC EXAMINATION; OTOACOUSTIC EMISSION; PERCEPTION DEAFNESS; PERIPHERAL NEUROPATHY; POINT MUTATION; PRIORITY JOURNAL; PROGNOSIS; VESTIBULAR DISORDER; VESTIBULAR TEST;

ADULT; FAMILY; HEARING LOSS; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; MALE; MIDDLE AGED; MYELIN PROTEINS; NEUROLOGIC EXAMINATION; POINT MUTATION; POLYMORPHISM, GENETIC; VESTIBULAR DISEASES; VESTIBULAR FUNCTION TESTS;

EID: 25644456185     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jns.2005.05.003     Document Type: Article

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