(Q28235848)

English

Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor

scientific article (publication date: December 1994)

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7881416%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7881416%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7881416%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

author name string

M Andrew

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7881416%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

S Jawad

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7881416%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

M J Owen

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7881416%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

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publication date

1 December 1994

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7881416%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

Human Molecular Genetics

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7881416%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7881416%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

12

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7881416%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

2175-2179

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7881416%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

Identifiers

10.1093/HMG/3.12.2175

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7881416%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7881416%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

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