S. Gu

Autosomal recessive retinitis pigmentosa locus RP 28 maps between D 2 S 1337 and D 2 S 286 on chromosome 2 p 11p 15 in an Indian family

C. Srikumari, A. Gal, G. Kumaramanickavel, 1999 .

Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy

Birgit Lorenz, Michael J. Denton, Ulrich Finckh, 1997, Nature Genetics.

Five novel mutations in the L1CAM gene in families with X linked hydrocephalus.

U Orth, W. Engel, E. Schwinger, 1996, Journal of medical genetics.

Autosomal recessive retinitis pigmentosa locusRP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian family

C. Srikumari, A. Gal, M. Denton, 1999, Journal of medical genetics.

Molecular analysis of the L1CAM gene in patients with X-linked hydrocephalus demonstrates eight novel mutations and suggests non-allelic heterogeneity of the trait.

J. Schröder, A. Gal, U. Orth, 1997, American journal of medical genetics.

Tubby-like protein-1 mutations in autosomal recessive retinitis pigmentosa

B. Lorenz, A. Lennon, A. Wright, 1998, The Lancet.

Early-onset severe rod-cone dystrophy in young children with RPE65 mutations.

B. Lorenz, M. Preising, A. Gal, 2000, Investigative ophthalmology & visual science.

Norrie-Warburg syndrome: two novel mutations in patients with classical clinical phenotype.

B. Grammatico, G. del Porto, A. Gal, 2009, Acta ophthalmologica Scandinavica. Supplement.