Gene Review:
RP25 - retinitis pigmentosa 25 (autosomal recessive)
Homo sapiens
This record was replaced with 346007.
- Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus. Abd El-Aziz, M.M., El-Ashry, M.F., Barragan, I., Marcos, I., Borrego, S., Antiñolo, G., Bhattacharya, S.S. Curr. Eye Res. (2005)
- Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin. Khaliq, S., Hameed, A., Ismail, M., Mehdi, S.Q., Bessant, D.A., Payne, A.M., Bhattacharya, S.S. Am. J. Hum. Genet. (1999)
- Mutation screening of three candidate genes, ELOVL5, SMAP1 and GLULD1 in autosomal recessive retinitis pigmentosa. Barragan, I., Marcos, I., Borrego, S., Antiñolo, G. Int. J. Mol. Med. (2005)
- Molecular cloning and characterization of human RAB23, a member of the group of Rab GTPases. Marcos, I., Borrego, S., Antiñolo, G. Int. J. Mol. Med. (2003)
- Molecular analysis of RIM1 in autosomal recessive Retinitis pigmentosa. Barragan, I., Marcos, I., Borrego, S., Antiñolo, G. Ophthalmic Res. (2005)
- Evaluation of the ELOVL4 gene in families with retinitis pigmentosa linked to the RP25 locus. Li, Y., Marcos, I., Borrego, S., Yu, Z., Zhang, K., Antiñolo, G. J. Med. Genet. (2001)