The role of Pax2 in mouse inner ear development (Q28595027)

1 February 2017

title

The role of Pax2 in mouse inner ear development (English)

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1 February 2017

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GOA release 2020-03-11

author name string

Quianna Burton

1

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1 February 2017

Laura K. Cole

2

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1 February 2017

Michael Mulheisen

3

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1 February 2017

Weise Chang

4

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1 February 2017

Doris K. Wu

5

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1 February 2017

language of work or name

English

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publication date

1 August 2004

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1 February 2017

published in

Developmental Biology

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1 February 2017

volume

272

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1 February 2017

issue

1

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1 February 2017

page(s)

161–175

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A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family

1 February 2017

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The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

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Identifiers

DOI

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1 February 2017

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