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Fisher, S. A. ; Rivera, A. ; Fritsche, L. G. ; Keilhauer, C. N. ; Lichtner, P. ; Meitinger, T. ; Rudolph, G. ; Weber, Bernhard H. F.

Case–control genetic association study of fibulin-6 (FBLN6 or HMCN1) variants in age-related macular degeneration (AMD)

Fisher, S. A., Rivera, A., Fritsche, L. G., Keilhauer, C. N., Lichtner, P., Meitinger, T. , Rudolph, G. and Weber, Bernhard H. F. (2007) Case–control genetic association study of fibulin-6 (FBLN6 or HMCN1) variants in age-related macular degeneration (AMD). Human Mutation 28 (4), pp. 406-413.

Date of publication of this fulltext: 11 Apr 2017 11:59
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Item typeArticle
Journal or Publication TitleHuman Mutation
Publisher:WILEY
Place of Publication:HOBOKEN
Volume:28
Number of Issue or Book Chapter:4
Page Range:pp. 406-413
Date2007
InstitutionsMedicine > Lehrstuhl für Humangenetik
Identification Number
ValueType
10.1002/humu.20464DOI
17216616PubMed ID
KeywordsCOMPLEMENT FACTOR-H; BEAVER DAM EYE; SUSCEPTIBILITY LOCI; GENOMEWIDE-SCAN; FAMILIAL AGGREGATION; EXTENDED FAMILIES; MACULOPATHY; RISK; POLYMORPHISM; POPULATION; age-related macular degeneration; fibulin-6; hemicentin-1; association; linkage disequilibrium; mutation; FBLN6; HMCN1
Dewey Decimal Classification600 Technology > 610 Medical sciences Medicine
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgPartially
Item ID35454

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