在RGS9或其基蛋白R9AP中存在缺陷,患者具有缓慢的光受体失活

Koji M Nishiguchi1, Michael A Sandberg, Aart C Kooijman

  • 1Ocular Molecular Genetics Institute, Harvard Medical School, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts 02114, USA.

Nature
|January 1, 2004
PubMed
概括

RGS9和R9AP蛋白对视力至关重要. 这些基因的突变会导致白视障碍,这种疾病的特征是光适应能力受损,看移动物体的能力降低.

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