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Ophthalmic Genetics

Volumn 22, Issue 2, 2001, Pages 107-115

Best's vitelliform macular dystrophy caused by a new mutation (val89ala) in the vmd2 gene

(5) Eksandh, L a Bakall, B a Bauer, B a Wadelius, C a Andreasson S a

a LUND UNIVERSITY HOSPITAL (Sweden)

Author keywords

Best's vitelliform macular dystrophy (BMD); Bestrophin; EOG (electro oculography); Macular degeneration; VMD2

Indexed keywords

AMINO ACID; BESTROPHIN; COMPLEMENTARY DNA; PROTEIN; UNCLASSIFIED DRUG;

ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; CHILD; CLINICAL ARTICLE; DIAGNOSTIC ERROR; ELECTROOCULOGRAPHY; ELECTRORETINOGRAPHY; EXON; EYE FUNDUS; EYE PHOTOGRAPHY; FEMALE; GENE LOCATION; GENE MUTATION; HUMAN; MALE; MEDICAL EXAMINATION; MOLECULAR GENETICS; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; RETINA MACULA VITELLIFORM DEGENERATION; SEQUENCE ANALYSIS; VISUAL ACUITY; VISUAL DISORDER;

ADOLESCENT; ADULT; AGED; CHILD; DNA; DNA MUTATIONAL ANALYSIS; ELECTROOCULOGRAPHY; EYE PROTEINS; FEMALE; FLUORESCEIN ANGIOGRAPHY; FUNDUS OCULI; HUMANS; MACULAR DEGENERATION; MALE; MIDDLE AGED; MUTATION; PEDIGREE; PHENOTYPE; VISUAL ACUITY;

EID: 0034828520 PISSN: 13816810 EISSN: None Source Type: Journal
DOI: 10.1076/opge.22.2.107.2226 Document Type: Article

Times cited : (31)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.