(Q28238064)

1

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Xiaoyun Jia

2

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Xiangming Guo

3

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Shiqiang Li

4

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Zhikuan Yang

5

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Qingjiong Zhang

Journal of Human Genetics

6

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language of work or name

English

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publication date

2006

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published in

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volume

51

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issue

7

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page(s)

634-40

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cites work

On- and off-responses in photopic electroretinogram in complete and incomplete types of congenital stationary night blindness

1 reference

12 December 2020

Species specific membrane anchoring of nyctalopin, a small leucine-rich repeat protein

1 reference

12 December 2020

X-linked high myopia associated with cone dysfunction.

1 reference

12 December 2020

Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type.

1 reference

12 December 2020

Molecular genetic study of congenital stationary night blindness

1 reference

12 December 2020

Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene.

1 reference

12 December 2020

Primate Retinal Signaling Pathways: Suppressing ON-Pathway Activity in Monkey With Glutamate Analogues Mimics Human CSNB1-NYX Genetic Night Blindness

1 reference

12 December 2020

Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1.

1 reference

12 December 2020

X-linked myopia in Danish family.

1 reference

12 December 2020

Linkage analysis of two families with X-linked recessive congenital motor nystagmus

1 reference

12 December 2020

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

1 reference

12 December 2020

Genotype-phenotype correlation in British families with X linked congenital stationary night blindness

1 reference

12 December 2020

Mutations in the CACNA1F and NYX genes in British CSNBX families

1 reference

12 December 2020

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6

1 reference

12 December 2020

Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness

1 reference

12 December 2020

Establishment of the concept of new clinical entities--complete and incomplete form of congenital stationary night blindness

1 reference

12 December 2020

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

1 reference

12 December 2020