Lessons from genetic studies of primary immunodeficiencies in a highly consanguineous population

Frontiers in Immunology

Volumn 8, Issue JUN, 2017, Pages

  Barbouche, Mohamed Ridha ^a,b   Mekki, Najla ^a,b   Ben Ali, Meriem ^a   Ben Mustapha, Imen ^a,b  

^a PASTEUR INSTITUTE OF TUNIS   (Tunisia)

^b UNIVERSITY OF TUNIS EL MANAR   (Tunisia)

Author keywords

Autosomal recessive; Consanguinity; Founder effect; Genetic counseling; Primary immunodeficiencies

Indexed keywords

PHOSPHOGLUCOMUTASE;

AUTOSOMAL RECESSIVE INHERITANCE; BARE LYMPHOCYTE SYNDROME; CONSANGUINEOUS MARRIAGE; FAMILY HISTORY; GENE; GENE MUTATION; GENETICS; HOMOZYGOSITY; HUMAN; HYPER IGE SYNDROME; IMMUNE DEFICIENCY; LEUKOCYTE ADHESION DEFICIENCY; LYMPHOPROLIFERATIVE DISEASE; OMENN SYNDROME; PHOSPHOGLUCOMUTASE 3 GENE; SHORT SURVEY;

EID: 85021722870     PISSN: None     EISSN: 16643224     Source Type: Journal    
DOI: 10.3389/fimmu.2017.00737     Document Type: Short Survey

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