A novel heterozygous loss‐of‐function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature-Reference-Cited by-同舟云学术

A novel heterozygous loss‐of‐function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature

Published:2019-11-07 Issue:1 Volume:182 Page:205-212
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Sagi‐Dain Lena¹^ORCID,Kurolap Alina²³^ORCID,Ilivitzki Anat³⁴,Mory Adi²,Paperna Tamar²,Kedar Reuven⁵,Gonzaga‐Jauregui Claudia⁶,Peleg Amir¹,Baris Feldman Hagit²³,

Affiliation:

1. Genetics Institute, Carmel Medical Center, Affiliated to the Ruth and Bruce Rappaport Faculty of Medicine Technion – Israel Institute of Technology Haifa Israel

2. The Genetics Institute Rambam Health Care Campus Haifa Israel

3. The Ruth and Bruce Rappaport Faculty of Medicine Technion – Israel Institute of Technology Haifa Israel

4. Pediatric Radiology Unit, Radiology Department Rambam Health Care Campus Haifa Israel

5. Obstetrics and Gynecology department Carmel Medical Center Haifa Israel

6. Regeneron Genetics Center Regeneron Pharmaceuticals Tarrytown New York USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61404

Reference26 articles.