Authors:
Maw, MA
Corbeil, D
Koch, J
Hellwig, A
Wilson-Wheeler, JC
Bridges, RJ
Kumaramanickavel, G
John, S
Nancarrow, D
Roper, K
Weigmann, A
Huttner, WB
Denton, MJ
Citation: Ma. Maw et al., A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration, HUM MOL GEN, 9(1), 2000, pp. 27-34
Authors:
Gu, SM
Kumaramanickavel, G
Srikumari, CR
Denton, MJ
Gal, A
Citation: Sm. Gu et al., Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S 1337 and D2S286 on chromosome 2p11-p15 in an Indian family, J MED GENET, 36(9), 1999, pp. 705-707