Novel ITGB2 Mutation Is Responsible for a Severe Form of Leucocyte Adhesion Deficiency Type 1.

Leukocyte adhesion deficiency type 1 (LAD1) is a rare autosomal recessive hereditary disorder characterized by recurrent infections, impaired pus formation, delayed wound healing, omphalitis, and delayed separation of the umbilical cord as hallmark features of the disease. It results from mutations...

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Publicado en:	BioMed Research International pp. 1 - 9
Autores principales:	Bouhouche, Ahmed, Tabache, Yasmin, Askander, Omar, Charoute, Hicham, Mesnaoui, Nada, Belayachi, Lamiae, El Hafidi, Naima, Hardizi, Houyam, El Fahime, Elmostafa, Erreimi, Naima, Barakat, Abdelhamid, Khattab, Mohammed, Seghrouchni, Fouad, El Hassani, Amine
Formato:	pictorial research tables/charts Journal Article
Publicado:	Wiley-Blackwell 3/3/2022
Acceso en línea:	Ver este registro en EBSCOhost