Disorders


 

MHC Class II Deficiency, Complementation Group B


 

OMIM

GeneLocusProtein
RFXANK19p12DNA-binding protein RFXANK

Laboratory Test Method Prenatal Carrier *
GENETAQ, Molecular Genetics Centre - Malaga, Spain• Sequence analysis of the entire coding region
  

* 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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