Disorders


 

Bare Lymphocyte Syndrome, Type II, Complementation Group A


 

OMIM

GeneLocusProtein
CIITA16p13MHC class II transactivator

Laboratory Test Method Prenatal Carrier *
GENETAQ, Molecular Genetics Centre - Malaga, Spain  

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

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