(Q30884957)

27 June 2017

title

ENU mutagenesis and the search for deafness genes (English)

1 reference

27 June 2017

1 reference

Hardisty RE

1

1 reference

27 June 2017

Mburu P

series ordinal

2

1 reference

27 June 2017

Brown SD

series ordinal

3

1 reference

27 June 2017

publication date

1 October 1999

1 reference

International Journal of Audiology

27 June 2017

number of pages

5

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

27 June 2017

volume

33

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27 June 2017

issue

5

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27 June 2017

page(s)

279-283

1 reference

A type VII myosin encoded by the mouse deafness gene shaker-1

27 June 2017

cites work

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

Dose-repetition increases the mutagenic effectiveness of N-ethyl-N-nitrosourea in mouse spermatogonia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

Positional cloning of the mouse circadian clock gene

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

Facing death in the fly: genetic analysis of apoptosis in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

Defective myosin VIIA gene responsible for Usher syndrome type 1B

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

The molecular basis of genetic dominance

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03005369909090110

10.3109/03005369909090110

21 January 2018

Identifiers

DOI

1 reference

release_yblqfksdfrbanhbs5tawujsr2q

27 June 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/yblqfksdfrbanhbs5tawujsr2q

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference