PedAM
Pediatric Disease Annotations & Medicines
| Disease | retinitis |
| Phenotype | C0004134|ataxia |
| Sentences | 5 |
| PubMedID- 21267618 | Posterior column ataxia with retinitis pigmentosa in a japanese family with a novel mutation in flvcr1. |
| PubMedID- 24753676 | Bassen and kornzweig first reported the association of ataxia with atypical retinitis pigmentosa (rp) and acanthocytosis in 1950. |
| PubMedID- 23475516 | In this review, we outline some of our recent efforts in the medical genome center at the university of tokyo hospital, including an identification of the causative gene for a mendelian disease (posterior column ataxia with retinitis pigmentosa), an approach to uncover susceptible genes for a non-mendelian disease (parkinson disease), and an application of exome sequencing for the molecular diagnosis of a disease with vast genetic heterogeneity (hereditary diffuse leukoencephalopathy with spheroids). |
| PubMedID- 24628582 | Autosomal recessive posterior column ataxia with retinitis pigmentosa caused by novel mutations in the flvcr1 gene. |
| PubMedID- 22277444 | We performed target capture and next-generation sequencing analyses of a small consanguineous family in which only two members were affected by posterior column ataxia with retinitis pigmentosa (pcarp). |
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