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Article

A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2.

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

Perandones Claudia, Micheli Federico E, Pellene Luis A, Bayly Marta A, Berkovic Samuel F, Dibbens Leanne M

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Share to Audiometry, Pure-Tone
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 22767442
DOI: 10.1002/mds.25083

Genes

SCARB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2.PMID 22767442Read ↗

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