Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone-Reference-Cited by-同舟云学术

Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone

Published:2015-02-20 Issue:11 Volume:24 Page:3286-3295
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Vallet Mahéva,Soares Dinesh C.,Wani Sachin,Sophocleous Antonia,Warner Jon,Salter Donald M.,Ralston Stuart H.,Albagha Omar M.E.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/24/11/3286/14143470/ddv068.pdf

Reference48 articles.

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2. Incidence and natural history of Paget's disease of bone in England and Wales;van Staa;J. Bone Miner. Res.,2002

3. Familial Paget's disease of bone: patterns of inheritance and frequency of linkage to chromosome 18q;Hocking;Bone,2000

4. Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35;Hocking;Am. J. Hum. Genet.,2001

5. Paget disease of bone: mapping of two loci at 5q35-qter and 5q31;Laurin;Am. J. Hum. Genet.,2001

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