Disorders


 

MELAS, MT-ND5-Related


Synonym(s): MELAS, MTND5-Related

 

OMIM

GeneLocusProtein
MT-ND5mitochondriaNADH-ubiquinone oxidoreductase chain 5

Laboratory Test Method Prenatal Carrier *
Athena Diagnostics Inc, Reference Lab - Worcester, MA, USA• Targeted mutation analysis
  
Centogene AG, Rare Disease Company - Rostock, Germany  
Centre Hospitalier Universitaire de Grenoble, Biochimie Genetique et Molculaire - Grenoble, France• Targeted mutation analysis
  
Charles University in Prague, First Faculty of Medicine - General University Hospital in Prague, Department of Pediatrics and Adolescent Medicine, Laboratory for Study of Mitochondrial Disorders - Prague, Czech Republic• Targeted mutation analysis
  
Columbia University, Molecular Neurogenetics Laboratory - New York, NY, USA• Targeted mutation analysis
  
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany• Targeted mutation analysis
  
Edith Wolfson Medical Center, Molecular Genetics Laboratory - Holon, Israel  
GeneDx - Gaithersburg, MD, USA• Targeted mutation analysis
  
Instituto de Medicina Genmica, IMEGEN - Paterna, Spain• Targeted mutation analysis
  
Pro Genetic, Inc, University Children's Genetics Laboratory - Glendale, CA, USA• Targeted mutation analysis
  
Radboud University Medical Centre, Laboratory of Genetic, Endocrine, and Metabolic Diseases - Nijmegen, Netherlands• Targeted mutation analysis
  
Rush University Medical Center, Genetics Laboratory - Department of Pathology - Chicago, IL, USA• Targeted mutation analysis
  
Sir Ganga Ram Hospital, Center of Medical Genetics - New Delhi, India• Targeted mutation analysis
  
Transgenomic, Transgenomic - Omaha - Omaha, NE, USA• Mutation scanning of the entire coding region
• Targeted mutation analysis
  

* 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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