(Q43277748)

PubMed publication ID

19747862

18 November 2017

title

Widespread retinal degenerative disease mutation (rdAc) discovered among a large number of popular cat breeds (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

14 May 2020

author name string

M Menotti-Raymond

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

14 May 2020

V A David

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

14 May 2020

S Pflueger

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

14 May 2020

M E Roelke

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

14 May 2020

J Kehler

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

14 May 2020

S J O'Brien

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

14 May 2020

K Narfström

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

14 May 2020

publication date

10 September 2009

1 reference

PubMed publication ID

19747862

18 November 2017

published in

The Veterinary Journal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

14 May 2020

volume

186

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

14 May 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

14 May 2020

page(s)

32-38

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndrome

14 May 2020

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7 January 2021

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7 January 2021

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12 December 2020

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Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

14 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6984347&resulttype=core&format=json

14 May 2020

PubMed publication ID

19747862

1 reference