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Search results 101 to 103 out of 103 for Setx

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HT Experiment

E-GEOD-61324 | Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2 [04_Cerebellum_and_brain]

Series Id:	GSE61324
Experiment Type:	transcription profiling by array
Study Type:	WT vs. Mutant
Source:	ArrayExpress

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DO Term

DOID:0050755 | spinocerebellar ataxia with axonal neuropathy 2

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Publication

37845749 | J:357886

First Author:	Bennett CL
Year:	2023
Journal:	Acta Neuropathol Commun
Title:	Senataxin helicase, the causal gene defect in ALS4, is a significant modifier of C9orf72 ALS G4C2 and arginine-containing dipeptide repeat toxicity.
Volume:	11
Issue:	1
Pages:	164

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