Clinically Significant Missense Variants in HumanGALNT3,GALNT8,GALNT12, andGALNT13Genes: Intriguing In Silico Findings-Reference-Cited by-同舟云学术

Clinically Significant Missense Variants in HumanGALNT3,GALNT8,GALNT12, andGALNT13Genes: Intriguing In Silico Findings

Published:2013-12-13 Issue:2 Volume:115 Page:313-327
ISSN:0730-2312
Container-title:Journal of Cellular Biochemistry
language:en
Short-container-title:J. Cell. Biochem.

Author:

Hussain Muhammad Ramzan M.¹,Nasir Jamal²,Al-Aama Jumana Yousuf¹

Affiliation:

1. Princess Al-Jawhara Al Brahim Center of Excellence in Research of Hereditary Disorders; Faculty of Medicine; King Abdulaziz University; Jeddah Kingdom of Saudi Arabia

2. Division of Biomedical Sciences (BMS), Human Genetics Research Centre; St. George's University of London (SGUL); London UK

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jcb.24666/fullpdf

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