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Results 1 - 10 of 12 for "Cardiomyopathy," mitochondrial
  1. HADHA gene 
    ... R, Mayatepek E, Bueltmann B, Korenke C. Intrauterine cardiomyopathy and cardiac mitochondrial proliferation in mitochondrial trifunctional protein (TFP) deficiency. Mol ...
    https://medlineplus.gov/genetics/gene/hadha - Genetics
  2. MT-TL1 gene 
    ... H, Honzik T, Zeman J, Linhart A. Hypertrophic cardiomyopathy due to the mitochondrial DNA mutation m.3303C>T diagnosed in an ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  3. MT-TK gene 
    ... alteration in the MT-TK gene results in cardiomyopathy, hearing loss, and other symptoms. mitochondrial tRNA-Lys MTTK trnK Tests of MT-TK ... Baram TZ, Madrid RE, DiMauro S. Maternally inherited cardiomyopathy and ... mutation in the mitochondrial tRNA(Lys) gene (G8363A). Am J Hum Genet. ...
    https://medlineplus.gov/genetics/gene/mt-tk - Genetics
  4. MT-TH gene 
    ... gene has been identified in several adults with cardiomyopathy, but without other common signs of mitochondrial disease such as neurological abnormalities. This mutation replaces ...
    https://medlineplus.gov/genetics/gene/mt-th - Genetics
  5. SLC25A4 gene 
    ... muscle-specific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy. Hum Mol Genet. 2005 Oct 15;14(20):3079-88. doi: 10.1093/hmg/ddi341. Epub 2005 Sep 9. Citation on PubMed ... 1 (ANT1): a new factor in mitochondrial disease. IUBMB Life. 2005 Sep;57(9):607- ...
    https://medlineplus.gov/genetics/gene/slc25a4 - Genetics
  6. DNAJC19 gene 
    ... R, Suomalainen A, Tyni T. New mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies. Pediatr Res. ...
    https://medlineplus.gov/genetics/gene/dnajc19 - Genetics
  7. TMEM70 gene 
    ... neurological problems can occur. Another common feature of mitochondrial complex V deficiency, especially when caused by TMEM70 gene mutations, is hypertrophic cardiomyopathy. This condition is characterized by thickening (hypertrophy) of ...
    https://medlineplus.gov/genetics/gene/tmem70 - Genetics
  8. MT-TV gene 
    ... mutation in tRNA(Val) is associated with hypertrophic cardiomyopathy and MELAS. ... valine transfer RNA gene of mitochondrial DNA. Ann Neurol. 1996 Sep;40(3):459- ...
    https://medlineplus.gov/genetics/gene/mt-tv - Genetics
  9. TAFAZZIN gene 
    ... a weakened immune system and recurrent infections. Dysfunctional mitochondria likely lead to ... This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/tafazzin - Genetics
  10. MLYCD gene 
    ... the cell where it is needed (such as mitochondria and peroxisomes).A lack of ... called cardiomyopathy. Byproducts of fatty acid processing build up in ...
    https://medlineplus.gov/genetics/gene/mlycd - Genetics
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