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The histidine decarboxylase model of tic pathophysiology: a new focus on the histamine H(3) receptor
Histamine dysregulation was implicated as a rare cause of Tourette syndrome and other tic disorders a decade ago by a landmark genetic study in a high density family pedigree, which implicated a hypomorphic mutation in the histidine decarboxylase (Hdc) gene as a rare but high penetrance genetic caus...
Gorde:
| Argitaratua izan da: | Br J Pharmacol |
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| Egile nagusia: | |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
John Wiley and Sons Inc.
2019
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7012946/ https://ncbi.nlm.nih.gov/pubmed/30714121 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bph.14606 |
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