Literature DB >> 5294608

Sex-linked myopic chorioretinal heredodegeneration.

J François, A De Rouck.   

Abstract

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Year:  1965        PMID： 5294608     DOI： 10.1016/0002-9394(65)92258-0

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN： 0002-9394            Impact factor:   5.258


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  3 in total

1.  Night blindness, characteristic facies, and skeletal abnormalities in two brothers.

Authors:  A G Hunter; D R Thompson; M H Reed; A G Macrodimitris
Journal:  J Med Genet       Date:  1979-08       Impact factor: 6.318

2.  A study of retinitis pigmentosa in the City of Birmingham. II Clinical and genetic heterogeneity.

Authors:  S Bundey; S J Crews
Journal:  J Med Genet       Date:  1984-12       Impact factor: 6.318

3.  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
  3 in total

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