New ocular phenotype associated with a mutation in the PAX2 gene (Q57199596)

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16 January 2020

title

New ocular phenotype associated with a mutation in the PAX2 gene (English)

1 reference

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16 January 2020

8

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16 January 2020

author name string

F Beby

1

1 reference

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16 January 2020

O Roche

2

1 reference

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16 January 2020

P Cochat

3

1 reference

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16 January 2020

B Ranchin

4

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16 January 2020

R Kohler

5

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16 January 2020

C Bonifas

6

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16 January 2020

M-P Cordier

7

1 reference

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16 January 2020

C Burillon

9

1 reference

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16 January 2020

P Denis

10

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16 January 2020

publication date

15 January 2010

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16 January 2020

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16 January 2020

volume

24

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16 January 2020

issue

7

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16 January 2020

page(s)

1293-1294

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Autosomal dominant optic nerve colobomas, vesicoureteral reflux, and renal anomalies.

16 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.330

Renal-coloboma syndrome: a multi-system developmental disorder caused by PAX2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.330

Redefining papillorenal syndrome: an underdiagnosed cause of ocular and renal morbidity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.330

Alterations in ocular surface and corneal thickness in relation to metabolic control in patients with chronic renal failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.2009.330

21 January 2018

Identifiers

DOI

10.1038/EYE.2009.330

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16 January 2020

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