A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataract

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• A novel truncation mutation in CRYBB1 associated with autosomal dominant congenital cataract with nystagmus
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• A Nonsense Mutation in CRYBB1 Associated with Autosomal Dominant Cataract Linked to Human Chromosome 22q
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• A CRYBB2 mutation in a Taiwanese family with autosomal dominant cataract
  Bằng: Yung-Hao Ching, et al.
  Được phát hành: (2019-01-01)