Literature DB >> 18188951

Clinical and genetic characterization of a Chinese family with CSNB1.

Ruifang Sui1, Fengrong Li, Jialiang Zhao, Ruxin Jiang.   

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Year:  2008        PMID： 18188951     DOI： 10.1007/978-0-387-74904-4_28

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN： 0065-2598            Impact factor:   2.622


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  3 in total

Review 1.  Nature and nurture: the complex genetics of myopia and refractive error.

Authors:  R Wojciechowski
Journal:  Clin Genet       Date:  2010-12-13       Impact factor: 4.438

Review 2.  Sequence features, structure, ligand interaction, and diseases in small leucine rich repeat proteoglycans.

Authors:  Norio Matsushima; Hiroki Miyashita; Robert H Kretsinger
Journal:  J Cell Commun Signal       Date:  2021-04-15       Impact factor: 5.782

3.  Two Novel NYX Gene Mutations in the Chinese Families with X-linked Congenital Stationary Night Blindness.

Authors:  Shuzhen Dai; Ming Ying; Kai Wang; Liming Wang; Ruifang Han; Peng Hao; Ningdong Li
Journal:  Sci Rep       Date:  2015-08-03       Impact factor: 4.379
  3 in total

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