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TRPM8 genetic variant is associated with chronic migraine and allodynia

TRPM8 genetic variant is associated with chronic migraine and allodynia

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_f2c9202349ae4541b5bf4eaa0198bec9

TRPM8 genetic variant is associated with chronic migraine and allodynia

About this item

Full title

TRPM8 genetic variant is associated with chronic migraine and allodynia

Publisher

Milan: Springer Milan

Journal title

Journal of headache and pain, 2019-12, Vol.20 (1), p.115-115, Article 115

Language

English

Formats

Publication information

Publisher

Milan: Springer Milan

More information

Scope and Contents

Contents

Background
Many single nucleotide polymorphisms (SNPs) have been reported to be associated with migraine susceptibility. However, evidences for their associations with migraine endophenotypes or subtypes are scarce. We aimed to investigate the associations of pre-identified migraine susceptibility loci in Taiwanese with migraine endophenotypes o...

Alternative Titles

Full title

TRPM8 genetic variant is associated with chronic migraine and allodynia

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_f2c9202349ae4541b5bf4eaa0198bec9

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_f2c9202349ae4541b5bf4eaa0198bec9

Other Identifiers

ISSN

1129-2369

E-ISSN

1129-2377

DOI

10.1186/s10194-019-1064-2

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