(Q34299469)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14970843%20AND%20SRC:MED&resulttype=core&format=json

23 November 2019

title

Genetic analysis of 2299delG and C759F mutations (USH2A) in patients with visual and/or auditory impairments (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14970843%20AND%20SRC:MED&resulttype=core&format=json

23 November 2019

4

1 reference

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23 November 2019

Amparo Navea

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14970843%20AND%20SRC:MED&resulttype=core&format=json

23 November 2019

author name string

Elena Aller

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14970843%20AND%20SRC:MED&resulttype=core&format=json

23 November 2019

Carmen Nájera

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14970843%20AND%20SRC:MED&resulttype=core&format=json

23 November 2019

José María Millán

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14970843%20AND%20SRC:MED&resulttype=core&format=json

23 November 2019

Herminio Pérez-Garrigues

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14970843%20AND%20SRC:MED&resulttype=core&format=json

23 November 2019

Concepción Vilela

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14970843%20AND%20SRC:MED&resulttype=core&format=json

23 November 2019

Magdalena Beneyto

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14970843%20AND%20SRC:MED&resulttype=core&format=json

23 November 2019

publication date

1 May 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14970843%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Human Genetics

23 November 2019

published in

1 reference

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23 November 2019

volume

12

1 reference

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23 November 2019

issue

5

1 reference

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23 November 2019

page(s)

407-410

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14970843%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201138

23 November 2019

exact match

0 references

cites work

Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201138

Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201138

Identification of novel USH2A mutations: implications for the structure of USH2A protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201138

Spectrum of mutations in USH2A in British patients with Usher syndrome type II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201138

A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201138

Mutations in myosin VIIA (MYO7A) and usherin (USH2A) in Spanish patients with Usher syndrome types I and II, respectively.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201138

Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201138