A de novo mutation in FMR1 in a patient with intellectual disability

Journal article

Peer reviewed

Sateesh Maddirevula, Hessa S. Alsaif, Niema Ibrahim and Fowzan S. Alkuraya

European journal of medical genetics, Vol.63(3), p.103763

01/03/2020

PMID: 31518692

Abstract

Genetics & Heredity

Life Sciences & Biomedicine

Science & Technology

1 Record Views

Title: A de novo mutation in FMR1 in a patient with intellectual disability
Creators - without role: Sateesh Maddirevula - King Faisal Specialist Hospital & Research Centre
Hessa S. Alsaif - King Faisal Specialist Hospital & Research Centre
Niema Ibrahim - King Faisal Specialist Hospital & Research Centre
Fowzan S. Alkuraya - Alfaisal University
Publication Details: European journal of medical genetics, Vol.63(3), p.103763
Publisher: Elsevier
Number of pages: 2
Grant note: Saudi Human Genome Program King Salman Center for Disability Research
Identifiers: 9918981908331
Academic Unit: King Faisal University; King Abdulaziz City for Science & Technology
Language: English
Resource Type: Journal article