Exome sequencing identifies novelNTRK1mutations in patients with HSAN-IV phenotype-Reference-Cited by-同舟云学术

Exome sequencing identifies novelNTRK1mutations in patients with HSAN-IV phenotype

Published:2017-03-22 Issue:4 Volume:173 Page:1009-1016
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Altassan Ruqaiah¹,Saud Haya Al²,Masoodi Tariq Ahmad²,Dosssari Haya Al²,Khalifa Ola¹³,Al-Zaidan Hamad¹⁴,Sakati Nadia¹,Rhabeeni Zuhair¹,Al-Hassnan Zuhair¹⁴,Binamer Yousef⁴⁵,Alhashemi Nadia⁶,Wade William⁷,Al-Zayed Zayed⁷,Al-Sayed Moeen¹,Al-Muhaizea Mohamed A.⁸,Meyer Brian²,Al-Owain Mohammad¹⁴,Wakil Salma M.²

Affiliation:

1. Department of Medical Genetics; King Faisal Specialist Hospital and Center Hospital; Riyadh Saudi Arabia

2. Department of Genetics; King Faisal Specialist Hospital and Research Center; Riyadh Saudi Arabia

3. Department of Pediatrics; Faculty of Medicine; Ain Shams University; Cairo Egypt

4. College of Medicine; Al-Faisal University; Riyadh Saudi Arabia

5. Department of Dermatology; King Faisal Specialist

6. Department of Pediatrics; Royal hospital; Muscat Oman

7. Department of Orthopedics; King Faisal Specialist Hospital and Research Center; Riyadh Saudi Arabia

8. Department of Neurology; King Faisal Specialist Hospital and Research Center; Riyadh Saudi Arabia

Funder

King Faisal Specialist Hospital and Research Center KFSHRC

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.38120/fullpdf

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