Rhizomelic Chondrodysplasia Punctata Type 1 Caused by a Novel Mutation in the PEX7 Gene-Reference-Cited by-同舟云学术

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Rhizomelic Chondrodysplasia Punctata Type 1 Caused by a Novel Mutation in the PEX7 Gene

Published:2015-03-05 Issue:1 Volume:7 Page:69-72
ISSN:1308-5727
Container-title:Journal of Clinical Research in Pediatric Endocrinology
language:
Short-container-title:Jcrpe

Author:

Çim Abdullah,Coşkun Salih,Görükmez Orhan,Yüksel Hatice,Uluca Ünal,Pietro Erminia Di,Plourde François,Braverman Nancy Elise

Publisher

Galenos Yayinevi

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Link

http://cms.galenos.com.tr/FileIssue/1/793/article/69-72.pdf

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genome Wide Analysis of WD40 Proteins in Saccharomyces cerevisiae and Their Orthologs in Candida albicans;The Protein Journal;2018-12-03

2. A Missense Mutation of G257A at Exon 3 in PEX7 CDS Was Responsible for the Incidence of Rhizomelic Chondrodysplasia Punctata Type 1;INT J PEDIATR-MASSHA;2018

3. Neonatal Rhizomelic Chondrodysplasia Punctata Type 1;Journal of Perinatal & Neonatal Nursing;2017-10

4. Chondrodysplasia Punctata;Diagnostic Imaging: Musculoskeletal Non-Traumatic Disease;2016

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