achromatopsia
英 [əkrəʊmə'tɒpsɪə] 美 [əˌkroʊmə'tɒpsɪr]

n.

色盲；全色盲；

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