A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients-Reference-Cited by-同舟云学术

A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients

Published:2017-10 Issue: Volume:90 Page:57-63
ISSN:0161-5890
Container-title:Molecular Immunology
language:en
Short-container-title:Molecular Immunology

Author:

Ben-Khemis Leila,Mekki Najla,Ben-Mustapha Imen,Rouault Karen,Mellouli Fethi,Khemiri Monia,Bejaoui Mohamed,Essaddam Leila,Ben-Becher Saayda,Boughamoura Lamia,Hassayoun Saida,Ben-Ali Meriem,Barbouche Mohamed-Ridha

Funder

Tunisian Ministry of Higher Education, Research and Technology

Publisher

Elsevier BV

Subject

Molecular Biology,Immunology

Reference20 articles.

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3. Clinical, immunological and genetic findings of a large Tunisian series of major histocompatibility complex class II deficiency patients;Ben-Mustapha;J. Clin. Immunol.,2013

4. A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients;Ben-Mustapha;Immunogenetics,2014

5. Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat;Brinkmann;Am. J. Hum. Genet.,1998

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