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                                       Details for article 17 of 17 found articles
 
 
  Whole-exome sequencing reveals a recurrent mutation in the cathepsin C gene that causes Papillon–Lefevre syndrome in a Saudi family
 
 
Title: Whole-exome sequencing reveals a recurrent mutation in the cathepsin C gene that causes Papillon–Lefevre syndrome in a Saudi family
Author: Alkhiary, Yaser Mohammad
Jelani, Musharraf
Almramhi, Mona Mohammad
Mohamoud, Hussein Sheikh Ali
Al-Rehaili, Rayan
Al-Zahrani, Hams Saeed
Serafi, Rehab
Yang, Huanming
Al-Aama, Jumana Yousuf
Appeared in: Saudi journal of biological sciences
Paging: Volume 23 (2016) nr. 5 pages 6 p.
Year: 2016
Contents:
Publisher: The Authors
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 17 of 17 found articles
 
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