A CpG Mutational Hotspot in a ONECUT Binding Site Accounts for the Prevalent Variant of Hemophilia B Leyden-Reference-Cited by-同舟云学术

A CpG Mutational Hotspot in a ONECUT Binding Site Accounts for the Prevalent Variant of Hemophilia B Leyden

Published:2013-03 Issue:3 Volume:92 Page:460-467
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Funnell Alister P.W.,Wilson Michael D.,Ballester Benoit,Mak Ka Sin,Burdach Jon,Magan Natisha,Pearson Richard C.M.,Lemaigre Frederic P.,Stowell Kathryn M.,Odom Duncan T.,Flicek Paul,Crossley Merlin

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference33 articles.

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2. Genotype analysis identifies the cause of the “royal disease”;Rogaev;Science,2009

3. Another genetic variant of haemophilia B: Haemophilia B Leyden;Veltkamp;Scand. J. Haematol.,1970

4. Hemophilia B Leyden: A sex-linked hereditary disorder that improves after puberty;Briët;N. Engl. J. Med.,1982

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