achromatopsia

听听怎么读
英 [əkrəʊmə'tɒpsɪə]
美 [əˌkroʊmə'tɒpsɪr]
是什么意思
  • n.

    色盲;全色盲;

  • 学习怎么用

    权威例句

    [Achromatopsia].
    ACHROMATOPSIA
    Achromatopsia
    A century of cerebral achromatopsia.
    Central achromatopsia: behavioral, anatomic, and physiologic aspects
    Restoration of cone vision in a mouse model of achromatopsia.
    Gene therapy rescues cone function in congenital achromatopsia
    Behavioral deficits and cortical damage loci in cerebral achromatopsia.
    CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia
    Cone Photoreceptor Function Loss-3, a Novel Mouse Model of Achromatopsia Due to a Mutation in Gnat2
    Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3.
    Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia
    Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy