A novel homozygous frameshift mutation in the DCC gene in a Pakistani family with autosomal recessive horizontal gaze palsy with progressive scoliosis‐2 with impaired intellectual development-Reference-Cited by-同舟云学术

A novel homozygous frameshift mutation in the DCC gene in a Pakistani family with autosomal recessive horizontal gaze palsy with progressive scoliosis‐2 with impaired intellectual development

Published:2020-11-03 Issue:2 Volume:185 Page:355-361
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Zaka Ayesha¹,Shahzad Shaheen¹^ORCID,Rao Hadi Zahid²,Hashim Yasmin¹,Basit Sulman³^ORCID

Affiliation:

1. Genomics Research Lab, Department of Biological Sciences International Islamic University Islamabad Pakistan

2. Department of Oral & Maxillofacial Surgery Bahria University Medical and Dental College Karachi Pakistan

3. Center for Genetics and Inherited Diseases Taibah University Medina Saudi Arabia

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61952

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