(Q45767747)

English

HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia.

scientific article published on 29 October 2012

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23043279

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23043279%20AND%20SRC:MED&resulttype=core&format=json

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10 March 2020

title

HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia (English)

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Europe PubMed Central

PubMed publication ID

23043279

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23043279%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

1 reference

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1 reference

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Europe PubMed Central

PubMed publication ID

23043279

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23043279%20AND%20SRC:MED&resulttype=core&format=json

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10 March 2020

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F Aminkeng

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1

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Europe PubMed Central

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23043279

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15 December 2017

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http://europepmc.org/abstract/MED/23043279

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29 October 2012

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23043279

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23043279%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

1 reference

Europe PubMed Central

PubMed publication ID

23043279

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23043279%20AND%20SRC:MED&resulttype=core&format=json

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10 March 2020

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83

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23043279

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23043279%20AND%20SRC:MED&resulttype=core&format=json

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10 March 2020

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1

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23043279

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23043279%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 March 2020

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31-32

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Europe PubMed Central

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23043279

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23043279%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

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https://api.crossref.org/works/10.1111%2FCGE.12030

retrieved

21 January 2018

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DOI

10.1111/CGE.12030

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23043279

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23043279%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 March 2020

PubMed publication ID

23043279

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23043279

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23043279%20AND%20SRC:MED&resulttype=core&format=json

(Q45767747)

HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia.

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