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Results 1 - 10 of 21 for Retinitis pigmentosa 25
  1. RHO gene 
    ... of the rhodopsin gene in one form of retinitis pigmentosa. Nature. 1990 Jan 25;343(6256):364-6. doi: 10.1038/343364a0. Citation on PubMed McAlear SD, Kraft TW, Gross AK. 1 rhodopsin mutations ... retinitis pigmentosa: implications for therapy. Trends Mol Med. 2005 Apr; ...
    https://medlineplus.gov/genetics/gene/rho - Genetics
  2. RPGR gene 
    ... within a new RPGR exon in X-linked retinitis pigmentosa. Nat Genet. 2000 Aug;25(4):462-6. doi: 10.1038/78182. Citation ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  3. TRNT1 deficiency 
    ... EM, Slusarski DC. Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis. Hum Mol Genet. 2016 Jan 1;25(1):44-56. doi: 10.1093/hmg/ddv446. ...
    https://medlineplus.gov/genetics/condition/trnt1-deficiency - Genetics
  4. TRNT1 gene 
    ... EM, Slusarski DC. Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis. Hum Mol Genet. 2016 Jan 1;25(1):44-56. doi: 10.1093/hmg/ddv446. ...
    https://medlineplus.gov/genetics/gene/trnt1 - Genetics
  5. Usher syndrome 
    ... El-Amraoui A. Usher syndrome (sensorineural deafness and retinitis pigmentosa): pathogenesis, molecular diagnosis and therapeutic approaches. Curr Opin Neurol. 2012 Feb;25(1):42-9. doi: 10.1097/WCO.0b013e32834ef8b2. ...
    https://medlineplus.gov/genetics/condition/usher-syndrome - Genetics
  6. Ataxia with vitamin E deficiency 
    ... gene in Italian families. Neurol Sci. 2004 Jul;25(3):130-7. doi: 10.1007/s10072-004-0246-z. Citation on PubMed Pang J, Kiyosawa M, Seko Y, Yokota T, Harino S, Suzuki J. Clinicopathological report of retinitis pigmentosa with vitamin E deficiency caused by mutation of ...
    https://medlineplus.gov/.../ataxia-with-vitamin-e-deficiency - Genetics
  7. PRPH2 gene 
    ... retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or ... Genet. 2004 Jun;25(2):133-45. doi: 10.1080/13816810490514388. Citation ...
    https://medlineplus.gov/genetics/gene/prph2 - Genetics
  8. Bardet-Biedl syndrome 
    Bardet-Biedl syndrome is a disorder that affects many parts of the body. The signs and symptoms of this condition vary among affected individuals, even among ...
    https://medlineplus.gov/genetics/condition/bardet-biedl-syndrome - Genetics
  9. TTPA gene 
    ... with the development of an eye disorder called retinitis pigmentosa that causes vision loss in people with ataxia ... T, Harino S, Suzuki J. Clinicopathological report of retinitis pigmentosa with vitamin E deficiency caused by mutation of ...
    https://medlineplus.gov/genetics/gene/ttpa - Genetics
  10. Abetalipoproteinemia 
    ... condition may also develop an eye disorder called retinitis pigmentosa, in which breakdown of the light-sensitive layer ( ... cause vision loss. In individuals with abetalipoproteinemia, the retinitis pigmentosa can result in complete vision loss. People with ...
    https://medlineplus.gov/genetics/condition/abetalipoproteinemia - Genetics
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