Autosomal dominant retinitis pigmentosa in a five-generation pedigree in People's Republic of China

Author:

Teng Y,Wang W,Tian H,Wang H,Hu X,Chen Y,Bittles A H

Publisher

Springer Science and Business Media LLC

Subject

Ophthalmology

Reference9 articles.

1. Hu DN . Genetic aspects of retinitis pigmentosa in China. Am J Med Genet 1982; 12: 51–56.

2. Pagon RA, Daiger SP . Retinitis pigmentosa overview. http://www.geneticclinics.org/profiles/rp-overview/details.html .

3. Van Soest S, Westerveld A, De Jong PTVM, Bleeker-Wagemakers EM, Bergen AAB . Retinitis pigmentosa: defined from a molecular point of view. Surv Ophthalmol 1999; 43: 321–334.

4. McGuire RE, Sullivan LS, Blanton SH, Church M, Heckenlively JR, Daiger SP . X-linked dominant cone–rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP15) to Xp22.13–p22.11. Am J Hum Genet 1995; 57: 87–94.

5. Marcos I, Ruiz A, Blaschak CJ, Vborrego S, Cutting GR, Antinolo G . Mutation analysis of GABRR1 and GABRR2 in autosomal recessive retinitis pigmentosa (rp25). J Med Genet 2000; 37: e5.

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