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Article

Comment: Autosomal dominant small vessel disease due to heterozygous HTRA1 mutations.

Neurology - 24 May 2016

Ihara Masafumi

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Share to HTRA1 gene
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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 27164690
DOI: 10.1212/WNL.0000000000002711

Genes

HTRA1

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Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease.Semantic proximity Read ↗

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