X chromosome exome sequencing reveals a novelALG13mutation in a nonsyndromic intellectual disability family with multiple affected male siblings-Reference-Cited by-同舟云学术

X chromosome exome sequencing reveals a novelALG13mutation in a nonsyndromic intellectual disability family with multiple affected male siblings

Author:

Bissar-Tadmouri Nesrine¹,Donahue Whithey L.²³,Al-Gazali Lihadh⁴,Nelson Stanley F.⁵,Bayrak-Toydemir Pinar²³,Kantarci Sibel⁶⁷

Affiliation:

1. Department of Biological and Environmental Sciences; Beirut Arab University; Tripoli Lebanon

2. ARUP Institute for Clinical and Experimental Pathology; Salt Lake City Utah

3. Department of Pathology; University of Utah; Salt Lake City Utah

4. Department of Pediatrics; United Arab Emirates University, College of Medicine; Al Ain United Arab Emirates

5. Department of Human Genetics; David Geffen School of Medicine at UCLA; Los Angeles California

6. Department of Pathology; Beth Israel Deaconess Medical Center; Boston Massachusetts

7. Harvard Medical School; Boston Massachusetts

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference28 articles.

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