SCOPUS 정보 검색 플랫폼

Volumn 23, Issue 10, 2000, Pages 1508-1514

Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness

(7) Dubourg, Odile a Barhoumi, Choukri a Azzedine, Hamid a Birouk, Nazha a Brice, Alexis a Bouche, Pierre a Leguern, Eric a

a PITIÉ SALPÊTRIÈRE HOSPITAL (France)

Author keywords

3q13 q22; 9q21 q22.3; Charcot Marie Tooth disease; Hereditary sensory neuropathy

Indexed keywords

ADULT; AGED; ARTICLE; CHROMOSOME 9Q; CLINICAL ARTICLE; FEMALE; FOOT ULCER; GENETIC LINKAGE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MUSCLE ATROPHY; MUSCLE WEAKNESS; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL;

ADULT; AGED; FEMALE; HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; HUMAN; LOD SCORE; MALE; MIDDLE AGE; MUSCLE WEAKNESS; NEURAL CONDUCTION; PHENOTYPE; SUPPORT, NON-U.S. GOV'T;

EID: 0033808833 PISSN: 0148639X EISSN: None Source Type: Journal
DOI: 10.1002/1097-4598(200010)23:10<1508::AID-MUS6>3.0.CO;2-D Document Type: Article

Times cited : (16)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.