Four USH2A Founder Mutations Underlie the Majority of Usher Syndrome Type 2 Cases among Non-Ashkenazi Jews-Reference-Cited by-同舟云学术

Four USH2A Founder Mutations Underlie the Majority of Usher Syndrome Type 2 Cases among Non-Ashkenazi Jews

Published:2008-06 Issue:2 Volume:12 Page:289-294
ISSN:1090-6576
Container-title:Genetic Testing
language:en
Short-container-title:Genetic Testing

Author:

Auslender Noa¹,Bandah Dikla²,Rizel Leah¹,Behar Doron M.³,Shohat Mordechai⁴,Banin Eyal²,Allon-Shalev Stavit⁵,Sharony Reuven⁶,Sharon Dror²,Ben-Yosef Tamar¹

Affiliation:

1. Department of Genetics and The Rappaport Family Institute for Research in the Medical Sciences, Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.

2. Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

3. Molecular Medicine Laboratory, Rambam Health Care Campus, Haifa, Israel.

4. Recanati Institute of Medical Genetics, Rabin & Schneider Medical Centers of Israel, Petah Tikva, Israel.

5. Genetics Institute, Ha'Emek Medical Center, Afula, Israel.

6. Genetics Institute, Sapir Medical Center-Meir Hospital, Kfar Saba, Israel.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical)

Link

http://www.liebertpub.com/doi/pdf/10.1089/gte.2007.0107

Reference23 articles.