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Article

A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure.

Movement disorders : official journal of the Movement Disorder Society - 1 Dec 2012

Guerrero-López Rosa, García-Ruiz Pedro J, Giráldez Beatriz G, Durán-Herrera Carmen, Querol-Pascual Maria Rosa, Ramírez-Moreno José María, Más Sebastián, Serratosa José M

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Share to Ataxia
Share to Lysosomal Membrane Proteins
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Myoclonic Epilepsies, Progressive

Share to Myoclonus

Share to Receptors, Scavenger

Share to Renal Insufficiency

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Source

Identifiers

PMID: 23225201
DOI: 10.1002/mds.25114

Genes

SCARB2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure.PMID 23225201Read ↗

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