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M. Litt

Department of Molecular and Medical Genetics

Oregon Health Sciences University

Portland 97201

USA

[email]@ohsu.edu

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Affiliation

Department of Molecular and Medical Genetics, Oregon Health Sciences University, Portland 97201, USA. 1997 - 1998

References

Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA. Litt, M., Kramer, P., LaMorticella, D.M., Murphey, W., Lovrien, E.W., Weleber, R.G. Hum. Mol. Genet. (1998) [Pubmed]
Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2. Litt, M., Carrero-Valenzuela, R., LaMorticella, D.M., Schultz, D.W., Mitchell, T.N., Kramer, P., Maumenee, I.H. Hum. Mol. Genet. (1997) [Pubmed]