Do heterozygous HTRA1 mutations carriers form a distinct clinical entity?-Reference-Cited by-同舟云学术

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Do heterozygous HTRA1 mutations carriers form a distinct clinical entity?

Published:2018-08-06 Issue:12 Volume:24 Page:1299-1300
ISSN:1755-5930
Container-title:CNS Neuroscience & Therapeutics
language:en
Short-container-title:CNS Neurosci Ther

Author:

Bougea Anastasia¹²^ORCID

Affiliation:

1. Center of Clinical, Experimental Surgery and Translational Research Biomedical Research Foundation of the Academy of Athens Athens Greece

2. 1st Department of Neurology National and Kapodistrian University of Athens, Medical School of Athens Athens Greece

Publisher

Wiley

Subject

Pharmacology (medical),Physiology (medical),Psychiatry and Mental health,Pharmacology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cns.13047

Reference6 articles.

1. Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease

2. Distinct molecular mechanisms ofHTRA1mutants in manifesting heterozygotes with CARASIL

3. HeterozygousHTRA1mutations are associated with autosomal dominant cerebral small vessel disease

4. Characterization of Heterozygous HTRA1 Mutations in Taiwanese Patients With Cerebral Small Vessel Disease

5. Histopathologic features of an autopsied patient with cerebral small vessel disease and a heterozygous HTRA1 mutation

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Heterozygous Pathogenic and Likely Pathogenic Symptomatic HTRA1 Variant Carriers in Cerebral Small Vessel Disease;International Journal of General Medicine;2023-03

2. Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review;Frontiers in Neurology;2022-12-22

3. HeterozygousHTRA1Mutations Cause Cerebral Small Vessel Diseases;Neurology Genetics;2022-12

4. Report of two pedigrees with heterozygous HTRA1 variants‐related cerebral small vessel disease and literature review;Molecular Genetics & Genomic Medicine;2022-08-10

5. Genotype–phenotype correlations of heterozygous HTRA1-related cerebral small vessel disease: case report and systematic review;neurogenetics;2021-05-08

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