Associated Papers
Combined immunodeficiency in a patient with c-Rel deficiency.
Beaussant-Cohen S et al.
The Journal of Allergy and Clinical Immunology, 2019
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.
Bakhchane A et al.
Plos One, 2017
28472130 (PubMed )
Supplement: pone.0176516.s002.xlsx › Feuil1
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