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BMJ Case Reports

Volumn , Issue , 2011, Pages

Alström syndrome - An uncommon cause of early childhood retinal dystrophy

(4) Sheck, Leo a Al Taie, Rasha b Sharp, Dianne b Vincent, Andrea a

a UNIVERSITY OF AUCKLAND (New Zealand)

b AUCKLAND DISTRICT HEALTH BOARD (New Zealand)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; CYTOSINE; THYMINE;

ALMS1 GENE; ALSTROM SYNDROME; AMINO ACID SUBSTITUTION; ARTICLE; BARDET BIEDL SYNDROME; CASE REPORT; CHILD; COLOR BLINDNESS; DIFFERENTIAL DIAGNOSIS; DISEASE SEVERITY; ELECTRORETINOGRAPHY; GENE; GENETIC ANALYSIS; HETEROZYGOSITY; HUMAN; HYPERMETROPIA; LCA GENE; LEBER CONGENITAL AMAUROSIS; MALE; MICROARRAY ANALYSIS; NONSENSE MUTATION; NYSTAGMUS; OPHTHALMOSCOPY; PATIENT REFERRAL; PRESCHOOL CHILD; PRIORITY JOURNAL; RETINA DYSTROPHY; SLIT LAMP; SPECTACLES; VISUAL IMPAIRMENT; VISUAL SYSTEM EXAMINATION;

EID: 80053072880 PISSN: None EISSN: 1757790X Source Type: Journal
DOI: 10.1136/bcr.06.2011.4388 Document Type: Article

Times cited : (4)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.