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2
7.3.471
7.3.471
http://dx.doi.org/10.1093/HMG/7.3.471
Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA
P356
Q24310410-2CE719F2-A9FE-40B0-8767-72B1338BBADA
P356
7.3.471
http://dx.doi.org/10.1093/HMG/7.3.471