A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families-Reference-Cited by-同舟云学术

A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families

Published:2020-08-28 Issue:11 Volume:182 Page:2570-2580
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Al‐Sulaiman Reem¹²,Othman Amna¹³^ORCID,El‐Akouri Karen¹³^ORCID,Fareed Shehab²^ORCID,AlMulla Hajer¹²^ORCID,Sukik Aseel⁴^ORCID,Al‐Mureikhi Mariam¹³,Shahbeck Noora¹³^ORCID,Ali Rehab¹³^ORCID,Al‐Mesaifri Fatma¹³^ORCID,Musa Sara¹^ORCID,Al‐Mulla Mariam¹³,Ibrahim Khalid⁵^ORCID,Mohamed Khalid⁵^ORCID,Al‐Nesef Maryam Ali⁶^ORCID,Ehlayel Mohammad⁷⁸^ORCID,Ben‐Omran Tawfeg¹³⁸^ORCID

Affiliation:

1. Department of Medical Genetics Hamad Medical Corporation Doha Qatar

2. Department of Adult Hematology/Oncology Hamad Medical Corporation Doha Qatar

3. Division of Genetic and Genomic Medicine Sidra Medicine Doha Qatar

4. Department of Internal Medicine Hamad Medical Corporation Doha Qatar

5. Division of Pediatric Neurology Sidra Medicine Doha Qatar

6. Department of Medicine Hamad Medical Corporation Doha Qatar

7. Department of Pediatrics Hamad Medical Corporation Doha Qatar

8. Weill Cornell Medical College Doha Qatar

Publisher

Wiley

Subject