(Q54532647)

31 May 2018

title

The D144E substitution in the VSX1 gene: a non-pathogenic variant or a disease causing mutation? (English)

1 reference

31 May 2018

author name string

Pras Eran

1

1 reference

31 May 2018

Abu Almogit

2

1 reference

31 May 2018

Zadok David

3

1 reference

31 May 2018

Haike Reznik Wolf

4

1 reference

31 May 2018

Garzozi Hana

5

1 reference

31 May 2018

Barkana Yaniv

6

1 reference

31 May 2018

Pras Elon

7

1 reference

31 May 2018

Avni Isaac

8

1 reference

31 May 2018

publication date

1 June 2008

1 reference

31 May 2018

published in

Ophthalmic Genetics

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31 May 2018

volume

29

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31 May 2018

issue

2

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31 May 2018

page(s)

53-59

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31 May 2018

Keratoconus and related noninflammatory corneal thinning disorders

cites work

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

The genetics of keratoconus

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

Familial keratoconus with cataract: linkage to the long arm of chromosome 15 and exclusion of candidate genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

Identification of a new locus for isolated familial keratoconus at 2p24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

Atopy and keratoconus: a multivariate analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

VSX1: a gene for posterior polymorphous dystrophy and keratoconus

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

No VSX1 gene mutations associated with keratoconus

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

Isolation and characterization of a novel human paired-like homeodomain-containing transcription factor gene, VSX1, expressed in ocular tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

Transcriptional activity of the paired-like homeodomain proteins CHX10 and VSX1

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

Risk factors and prognosis for corneal ectasia after LASIK.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810802008242

10.1080/13816810802008242

21 January 2018

Identifiers

DOI

1 reference

31 May 2018

1 reference

31 May 2018