Literature DB >> 4537233

The autosomal recessive variety of congenital stationary night-blindness with myopia.

V M Der Kaloustian, S A Baghdassarian.   

Abstract

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Year:  1972        PMID： 4537233      PMCID： PMC1469195          DOI： 10.1136/jmg.9.1.67

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  1 in total

1.  Syndrome of congenital high myopia with nyctalopia. Report of findings in 25 families.

Authors:  S Merin; H Rowe; E Auerbach; J Landau
Journal:  Am J Ophthalmol       Date:  1970-10       Impact factor: 5.258
  1 in total
  1 in total

1.  A naturally-occurring mutation in Cacna1f in a rat model of congenital stationary night blindness.

Authors:  Yonghao Gu; Lifeng Wang; Jie Zhou; Qun Guo; Na Liu; Zhenqiang Ding; Li Li; Xinping Liu; Jing An; Guolin Yan; Libo Yao; Zuoming Zhang
Journal:  Mol Vis       Date:  2008-01-09       Impact factor: 2.367
  1 in total

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