Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2016 | 1 |
2017 | 1 |
2024 | 0 |
PubMed (cited) for id: 617507
2 results
Results by year
Filters applied: . Clear all
Page 1
ZNHIT3 is defective in PEHO syndrome, a severe encephalopathy with cerebellar granule neuron loss.
Brain. 2017 May 1;140(5):1267-1279. doi: 10.1093/brain/awx040.
Brain. 2017.
PMID: 28335020
CCDC88A mutations cause PEHO-like syndrome in humans and mouse.
Nahorski MS, Asai M, Wakeling E, Parker A, Asai N, Canham N, Holder SE, Chen YC, Dyer J, Brady AF, Takahashi M, Woods CG.
Nahorski MS, et al.
Brain. 2016 Apr;139(Pt 4):1036-44. doi: 10.1093/brain/aww014. Epub 2016 Feb 25.
Brain. 2016.
PMID: 26917597
Free PMC article.
Item in Clipboard
Cite
Cite