Litt M.,1998
Litt M., Kramer P., LaMorticella D.M., Murphey W., Lovrien E.W., Weleber R.G. Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA. - Hum.Mol.Genet., 1998, v. 7, p. 471-474.
Litt M., Kramer P., LaMorticella D.M., Murphey W., Lovrien E.W., Weleber R.G. Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA. - Hum.Mol.Genet., 1998, v. 7, p. 471-474.
