This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

Comment

. 1998 Jan;18(1):11-2.

doi: 10.1038/ng0198-11.

Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR

A Martínez-Mir, E Paloma, R Allikmets, C Ayuso, T del Rio, M Dean, L Vilageliu, R Gonzàlez-Duarte, S Balcells

PMID: 9425888
DOI: 10.1038/ng0198-11

Free article

Comment

Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR

A Martínez-Mir et al. Nat Genet. 1998 Jan.

Free article

. 1998 Jan;18(1):11-2.

doi: 10.1038/ng0198-11.

Authors

A Martínez-Mir, E Paloma, R Allikmets, C Ayuso, T del Rio, M Dean, L Vilageliu, R Gonzàlez-Duarte, S Balcells

PMID: 9425888
DOI: 10.1038/ng0198-11

No abstract available

PubMed Disclaimer

Comment on

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.
Allikmets R, Singh N, Sun H, Shroyer NF, Hutchinson A, Chidambaram A, Gerrard B, Baird L, Stauffer D, Peiffer A, Rattner A, Smallwood P, Li Y, Anderson KL, Lewis RA, Nathans J, Leppert M, Dean M, Lupski JR. Allikmets R, et al. Nat Genet. 1997 Mar;15(3):236-46. doi: 10.1038/ng0397-236. Nat Genet. 1997. PMID: 9054934

Publication types

Actions
Actions
Actions

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

Substances

Actions
Actions

LinkOut - more resources

Full Text Sources
- Digital CSIC Spanish National Research Council - Access Free Full Text
- Nature Publishing Group
Other Literature Sources
- The Lens - Patent Citations Database
Molecular Biology Databases
- BioCyc