A HomozygousNme7Mutation Is Associated withSitus Inversus Totalis-Reference-Cited by-同舟云学术

A HomozygousNme7Mutation Is Associated withSitus Inversus Totalis

Published:2016-05-09 Issue:8 Volume:37 Page:727-731
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Reish Orit¹²,Aspit Liam³,Zouella Arielle³,Roth Yehudah²⁴,Polak-Charcon Sylvie⁵,Baboushkin Tatiana²⁵,Benyamini Lilach¹,Scheetz Todd E.⁶,Mussaffi Huda²⁷,Sheffield Val C.⁸,Parvari Ruti³⁹

Affiliation:

1. Genetic Institute; Assaf Harofeh Medical Center; Zerifin Israel

2. The Sackler School of Medicine; Tel Aviv University; Tel Aviv Israel

3. Shraga Segal Department of Microbiology; Immunology and Genetics, Faculty of Health Sciences; Ben-Gurion University of the Negev; Beer Sheva Israel

4. Department of Otolaryngology - Head and Neck Surgery; Edith Wolfson Medical Center; Holon Israel

5. Department of Pathology; The Sheba Medical Center at Tel Hashomer; Ramat Gan Israel

6. Stephen A Wynn Institute for Vision Research and Department of Ophthalmology and Visual Sciences; University of Iowa; Iowa City Iowa

7. Pediatric Pulmunology Institute; Schneider Children's Medical Center of Israel; Petach Tikva Israel

8. Department of Pediatrics, Division of Medical Genetics; University of Iowa; Iowa City Iowa

9. National Institute of Biotechnology in the Negev; Ben-Gurion University of the Negev; Beer Sheva Israel

Funder

United States - Israel Binational Science Foundation

National Institutes of Health

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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4. Nme protein family evolutionary history, a vertebrate perspective;Desvignes;BMC Evol Biol,2009

5. A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia;Duriez;Proc Natl Acad Sci U S A,2007

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