Retinitis Pigmentosa 41

mutations in PROM1; aka RP41

Also Known As:

Retinal Degeneration, Autosomal Recessive, Prominin-Related

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

1.	Macular Degeneration (Age-Related Maculopathy)
2.	Cone-Rod Dystrophy 12
3.	Stargardt disease 4

1.	Lima de Carvalho, Jose Ronaldo: 1 article (12/2019)
2.	Mahajan, Vinit B: 1 article (12/2019)
3.	Maumenee, Irene H: 1 article (12/2019)
4.	Park, Karen Sophia: 1 article (12/2019)
5.	Ragi, Sara D: 1 article (12/2019)
6.	Tanaka, Akemi J: 1 article (12/2019)
7.	Tsang, Stephen H: 1 article (12/2019)

Drugs and Important Biological Agents (IBA) related to Retinitis Pigmentosa 41:

1.	Retinaldehyde (Retinal)IBA 12/01/2019 - "Mutations in PROM1 are typically associated with cone-rod dystrophy 12 (OMIM#3612657), autosomal dominant retinal macular dystrophy 2 (OMIM#608051), autosomal recessive retinitis pigmentosa 41 (OMIM#612095), and Stargardt disease 4 (OMIM#603786). "