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Article

The E646D-ATP13A4 mutation associated with autism reveals a defect in calcium regulation.

Cellular and molecular neurobiology - 1 Mar 2010

Vallipuram Janaki, Grenville Jeffrey, Crawford Dorota A

Abstract excerpt

ATP13A4 is a member of the subfamily of P5-type ATPases. P5-type ATPases are the least studied of the P-type ATPase subfamilies with no ion specificities assigned to them. In order to elucidate ATP13A4 function, we studied the protein's subcellular localization and tested whether it is involved i...

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PMID: 19731010
DOI: 10.1007/s10571-009-9445-8

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-19731010-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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