Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease-Reference-Cited by-同舟云学术

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Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease

Published:2008-09 Issue:9 Volume:10 Page:675-684
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Kaya Namik,Imtiaz Faiqa,Colak Dilek,Al-Sayed Moeenaldeen,Al-Odaib Ali,Al-Zahrani Fatma,Al-Mubarak Bashayer R.,Al-Owain Mohammad,Al-Dhalaan Hesham,Chedrawi Aziza,Al-Hassnan Zuhair,Coskun Serdar,Sakati Nadia,Ozand Pinar,Meyer Brian F.

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference44 articles.

Cited by 16 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. Cellular and molecular mechanisms of aspartoacylase and its role in Canavan disease;Cell & Bioscience;2024-04-06

2. Identification of novel genomic imbalances in Saudi patients with congenital heart disease;Molecular Cytogenetics;2018-01-25

3. Canavan disease: An Arab scenario;Gene;2015-04

4. Pinar T. Ozand;Journal of Child Neurology;2013-10-01

5. A novel syndrome of abnormal striatum and congenital cataract: evidence for linkage to chromosomes 11;Clinical Genetics;2012-12-21

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