Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1 , Associated with Autosomal‐Dominant Hereditary Connective Tissue Disease-Reference-Cited by-同舟云学术

Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1 , Associated with Autosomal‐Dominant Hereditary Connective Tissue Disease

Published:2015-11-04 Issue:1 Volume:37 Page:84-97
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Capuano Alessandra¹,Bucciotti Francesco¹,Farwell Kelly D.²,Tippin Davis Brigette²,Mroske Cameron²,Hulick Peter J.³,Weissman Scott M.³,Gao Qingshen⁴,Spessotto Paola¹,Colombatti Alfonso¹,Doliana Roberto¹

Affiliation:

1. Department of Translational Research CRO‐IRCCS National Cancer Institute Aviano 33081 Italy

2. Ambry Genetics Aliso Viejo California 92656

3. Center for Medical Genetics NorthShore University HealthSystem Evanston Illinois 60201

4. NorthShore Research Institute NorthShore University HealthSystem Evanston Illinois 60201

Funder

AIRC (Associazione Italiana per la Ricerca sul Cancro)

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.22920

Reference57 articles.

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