Disorders


 

KIF1B-Related Pheochromocytoma


 

OMIM

GeneLocusProtein
KIF1B1p36.22 

Laboratory Test Method Prenatal Carrier *
Harvard Medical School and Partners Healthcare, Laboratory for Molecular Medicine - Cambridge, MA, USA• 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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