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American Journal of Human Genetics

Volumn 90, Issue 5, 2012, Pages 934-

Documenting the corneal phenotype associated with the MIR184 c.57C>T mtation

(3) Iliff, Benjamin W a Riazuddin, S Amer a Gottsch, John D a

a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MICRORNA; MICRORNA 184; UNCLASSIFIED DRUG;

ANTERIOR EYE SEGMENT; BIOMICROSCOPY; CHROMOSOME 15Q; CONGENITAL CATARACT; CONGENITAL CORNEA DYSTROPHY; EDICT SYNDROME; GENE MUTATION; GENETIC ASSOCIATION; IRIS DISEASE; KERATOCONUS; LETTER; PENETRATING KERATOPLASTY; PHENOTYPE; PRIORITY JOURNAL; SLIT LAMP;

CATARACT; CHROMOSOMES, HUMAN, PAIR 15; FEMALE; GENETIC LINKAGE; HUMANS; KERATOCONUS; MALE;

EID: 84860710724 PISSN: 00029297 EISSN: 15376605 Source Type: Journal
DOI: 10.1016/j.ajhg.2012.01.019 Document Type: Letter

Times cited : (7)

References (6)

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2
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3
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- DOI 10.1167/iovs.03-0399
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6
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.