SCOPUS 정보 검색 플랫폼

Volumn 101, Issue 2, 2001, Pages 181-183

From DFNB2 to usher syndrome: Variable expressivity of the same disease [4]

(7) Zina, Zeineb Ben a Masmoudi, Saber b Ayadi, Hammadi b Chaker, Fakher a Ghorbel, Abdel Monem a Drira, Mohamed a Petit, Christine c

a Service d'Ophtalmologie (Tunisia)

b UNIVERSITY OF SFAX (Tunisia)

c INSTITUT PASTEUR (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; CHILD; CLINICAL ARTICLE; CONSANGUINEOUS MARRIAGE; FEMALE; GENE EXPRESSION; GENE LOCUS; GENE MUTATION; HEARING LOSS; HUMAN; LETTER; MALE; NIGHT BLINDNESS; PHENOTYPE; PRIORITY JOURNAL; RETINA DYSTROPHY; SYNDROME DELINEATION; TUNISIA; USHER SYNDROME; VESTIBULAR DISORDER;

ADOLESCENT; ADULT; AGED; CHILD; DYNEIN ATPASE; FEMALE; FOLLOW-UP STUDIES; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MIDDLE AGED; MUTATION; MYOSINS; RETINITIS PIGMENTOSA;

EID: 0035877147 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.1335 Document Type: Letter

Times cited : (43)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.