Clinical and molecular studies in a family with probable X-linked dominant Charcot-Marie-Tooth disease involving the central nervous system

Archives of Neurology

Volumn 58, Issue 11, 2001, Pages 1891-1896

  Hisama, Fuki M ^a   Lee, Helen H ^a   Vashlishan, Amy ^a   Tekumalla, Poornima ^a   Russell, David S ^a   Auld, Elizabeth ^b   Goldstein, Jonathan M ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b VA CONNECTICUT HEALTHCARE SYSTEM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 32; PROTEOLIPID;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CLINICAL FEATURE; ELECTROPHYSIOLOGY; FEMALE; GENETIC ANALYSIS; GENOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; HYPERREFLEXIA; MALE; NERVE CONDUCTION; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; PROMOTER REGION; SEQUENCE ANALYSIS; SEX DIFFERENCE; SPASTICITY; X CHROMOSOME; X CHROMOSOME DOMINANT INHERITANCE;

EID: 0034756995     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.58.11.1891     Document Type: Article

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