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Article

CARASIL families from India with 3 novel null mutations in the HTRA1 gene.

Neurology - 5 Dec 2017

Preethish-Kumar Veeramani, Nozaki Hiroaki, Tiwari Sarbesh, Vengalil Seena, Bhat Maya, Prasad Chandrajit, Onodera Osamu, Uemura Masahiro, Doniparthi Seshagiri, Saini Jitender, Nashi Saraswati, Polavarapu Kiran, Nalini Atchayaram

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Identifiers

PMID: 29101275
DOI: 10.1212/WNL.0000000000004710

Genes

HTRA1

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

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CARASIL families from India with 3 novel null mutations in the HTRA1 gene.PMID 29101275Read ↗

Two novel HTRA1 mutations in a European CARASIL patient.Semantic proximity Read ↗

A novel mutation in the HTRA1 gene identified in Chinese CARASIL pedigree.Semantic proximity Read ↗

A missense <i>HTRA1</i> mutation expands CARASIL syndrome to the Caucasian populationSemantic proximity Read ↗

A novel HTRA1 exon 2 mutation causes loss of protease activity in a Pakistani CARASIL patient.Semantic proximity Read ↗

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A Chinese CARASIL Patient Caused by Novel Compound Heterozygous Mutations in HTRA1.Semantic proximity Read ↗

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