A New Patient with Inherited TYK2 Deficiency
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DOI: 10.1007/s10875-019-00713-5
Abstract: Complete TYK2 deficiency (IMMUNODEFICIENCY 35 OMIM (611521)) is a rare disorder, inherited as an autosomal recessive (AR) trait, which has been previously described in nine patients from seven unrelated kindreds [1–3]. It was first reported… read more here.
Keywords: complete tyk2; hyper ige; deficiency; tyk2 deficiency ... See more keywords