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Article

DYT2 revealed: Hippocalcin mutations cause autosomal-recessive isolated dystonia.

Movement disorders : official journal of the Movement Disorder Society - 1 Nov 2015

Erro Roberto, Klein Christine

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 26094611
DOI: 10.1002/mds.26280

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DYT2 revealed: Hippocalcin mutations cause autosomal-recessive isolated dystonia.PMID 26094611Read ↗

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Novel Dystonia Genes: Clues on Disease Mechanisms and the Complexities of High‐Throughput SequencingSemantic proximity Read ↗

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Inherited isolated dystonia: clinical genetics and gene function.Semantic proximity Read ↗

Specific Cognitive Changes due to Hippocalcin Alterations? A Novel Familial Homozygous Hippocalcin Variant Associated with Inherited Dystonia and Altered Cognition.Semantic proximity Read ↗

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