Disorders


 

Hereditary Motor and Sensory Neuropathy VI


Synonym(s): Charcot-Marie-Tooth Disease Type 6, CMT6, HMSN VI, HMSN6

 

OMIM

GeneLocusProtein
MFN21p36.22Mitofusin-2

Laboratory Test Method Prenatal Carrier *
Academic Medical Center, Department of Genome Analysis and Laboratory for Neurogenetics - Amsterdam, Netherlands  
CGC Genetics - Porto, Portugal  
Medical Neurogenetics - Atlanta, GA, USA  
Southmead Hospital - Pathology Sciences, Bristol Genetics Laboratory - North Bristol NHS Trust - Bristol, Great Britain  

* 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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