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Article

Unraveling Phenotypic Variability in Action Myoclonus with Renal Failure with SCARB2 Mutation in Siblings.

Movement disorders clinical practice - 1 Aug 2024

Nair Lakshmi J, Vijayaraghavan Asish

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 38741477
DOI: 10.1002/mdc3.14067
PMCID: PMC11329563

Genes

SCARB2

Provenance

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Unraveling Phenotypic Variability in Action Myoclonus with Renal Failure with SCARB2 Mutation in Siblings.PMID 38741477Read ↗

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