DetectingPKD1variants in polycystic kidney disease patients by single-molecule long-read sequencing-Reference-Cited by-同舟云学术

DetectingPKD1variants in polycystic kidney disease patients by single-molecule long-read sequencing

Published:2017-05-29 Issue:7 Volume:38 Page:870-879
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Borràs Daniel M.¹²³^ORCID,Vossen Rolf H. A. M.⁴,Liem Michael⁴,Buermans Henk P. J.⁴,Dauwerse Hans⁵,van Heusden Dave⁵,Gansevoort Ron T.⁶,den Dunnen Johan T.⁴⁵⁷,Janssen Bart¹,Peters Dorien J. M.⁵,Losekoot Monique⁷,Anvar Seyed Yahya⁴⁵

Affiliation:

1. GenomeScan B.V; Leiden The Netherlands

2. Institut National de la Santé et de la Recherche Médicale (INSERM); Institut of Cardiovascular and Metabolic Disease; Toulouse France

3. Université Toulouse III Paul-Sabatier; Toulouse France

4. Leiden Genome Technology Center (LGTC); Department of Human Genetics; Leiden University Medical Center (LUMC); Leiden The Netherlands

5. Department of Human Genetics; Leiden University Medical Center (LUMC); Leiden The Netherlands

6. Department of Nephrology; University Hospital Groningen; University Medical Center Groningen; Groningen The Netherlands

7. Department of Clinical Genetics; Leiden University Medical Center (LUMC); Leiden The Netherlands

Funder

Seventh Framework Programme

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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