英语词汇“night blindness”的意思、用法、释义、翻译、读音、例句、短语、词组-英语词典

是什么意思

夜盲；雀目；

英英释义

night blindness

n.inability to see clearly in dim light; due to a deficiency of vitamin A or to a retinal disorder
同义词：nyctalopiamoon blindness

学习怎么用

双语例句

Night blindness is most likely caused by vision problems.
夜盲很有可能由视觉问题所引起。
Too few proteins lead to night blindness and xerophthalmia.
蛋白质不足可导致夜盲和干眼病。

权威例句

Night blindness
Night Blindness
NIGHT BLINDNESS.
Congenital stationary night blindness with negative electroretinogram. A new classification
The Briard dog: a new animal model of congenital stationary night blindness.
Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness.
A naturally occurring mouse model of X-linked congenital stationary night blindness.
Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness.
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night...

单词	night blindness
释义	night blindness 听听怎么读英 [nait ?bla?ndn?s] 美 [na?t ?bla?ndn?s] 是什么意思 n. 夜盲；雀目；英英释义 night blindness n.inability to see clearly in dim light; due to a deficiency of vitamin A or to a retinal disorder 同义词：nyctalopiamoon blindness 学习怎么用双语例句 Night blindness is most likely caused by vision problems. 夜盲很有可能由视觉问题所引起。 Too few proteins lead to night blindness and xerophthalmia. 蛋白质不足可导致夜盲和干眼病。权威例句 Night blindness Night Blindness NIGHT BLINDNESS. Congenital stationary night blindness with negative electroretinogram. A new classification The Briard dog: a new animal model of congenital stationary night blindness. Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness. A naturally occurring mouse model of X-linked congenital stationary night blindness. Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness. Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night...
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