Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21q

Author:

Mackay Donna S,Andley Usha P,Shiels Alan

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference60 articles.

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2. Sommer A, Tielsch JM, Katz J et al: Racial differences in the cause-specific prevalence of blindness in east Baltimore. N Engl J Med 1991; 325: 1412–1417.

3. Francois J : Genetics of cataract. Ophthalmologica 1982; 184: 61–71.

4. Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/Omim .

5. Eiberg H, Lund AM, Warburg M, Rosenberg T : Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36. Hum Genet 1995; 96: 33–38.

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