Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA

Author: Litt M.  

Publisher: Oxford University Press

E-ISSN: 0964-6906|7|3|471-474

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.7, Iss.3, 1998-03, pp. : 471-474

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