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Results 1 - 5 of 5 for "Maternally-inherited" mitochondrial myopathy
  1. MT-TE gene 
    ... TE gene are also involved in infantile transient mitochondrial myopathy (also known as benign COX deficiency myopathy). This ... or 3.The mutations involved in infantile transient mitochondrial myopathy change single nucleotides in mitochondrial DNA. Specifically, the ...
    https://medlineplus.gov/genetics/gene/mt-te - Genetics
  2. Mitochondrial Disorders From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Muscle Disorders/Specifics ... Muscle Disorders ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... Degenerative Nerve Diseases/Specifics ... Degenerative Nerve ...
    https://www.ninds.nih.gov/.../disorders/mitochondrial-disorders - External Health Links
  3. MT-TL1 gene 
    ... one mutation in the MT-TL1 gene causes maternally inherited diabetes and deafness (MIDD). People with this condition ... New insights in the molecular pathogenesis of the maternally inherited diabetes and deafness syndrome. Endocrinol Metab Clin North ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  4. MT-TK gene 
    ... found in a small number of people with maternally inherited diabetes and deafness (MIDD), which is a condition ... Shanske S, Baram TZ, Madrid RE, DiMauro S. Maternally inherited cardiomyopathy and hearing loss associated with a novel ...
    https://medlineplus.gov/genetics/gene/mt-tk - Genetics
  5. Mitochondrial DNA 
    ... PubMed Central Guan MX. Molecular pathogenetic mechanism of maternally inherited deafness. Ann N Y Acad Sci. 2004 Apr; ... on PubMed Central Van Camp G, Smith RJ. Maternally inherited hearing impairment. Clin Genet. 2000 Jun;57(6): ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics