Published in
Wiley, The American Journal of Medical Genetics - Part A, 11(182), p. 2570-2580, 2020
DOI: 10.1002/ajmg.a.61829
Links
Tools
A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families
Journal article published in 2020 by
Reem Al‐Sulaiman,
Amna Othman 
,
Karen El‐Akouri ,
Shehab Fareed ,
Hajer AlMulla ,
Aseel Sukik ,
Mariam Al‐Mureikhi,
Noora Shahbeck ,
Rehab Ali ,
Fatma Al‐Mesaifri ,
Sara Musa ,
Mariam Al‐Mulla,
Khalid Ibrahim ,
Khalid Mohamed ,
Maryam Ali Al‐Nesef
and other authors.
,
Karen El‐Akouri ,
Shehab Fareed ,
Hajer AlMulla ,
Aseel Sukik ,
Mariam Al‐Mureikhi,
Noora Shahbeck ,
Rehab Ali ,
Fatma Al‐Mesaifri ,
Sara Musa ,
Mariam Al‐Mulla,
Khalid Ibrahim ,
Khalid Mohamed ,
Maryam Ali Al‐Nesef
and other authors.
This paper is made freely available by the publisher.
Full text: Download
Published version:
archiving forbidden
Data provided by 