HTRA1-related autosomal dominant cerebral small vessel disease

Jing-Yi LIU; Yi-Cheng ZHU; Li-Xin ZHOU; Yan-Ping WEI; Chen-Hui MAO; Li-Ying CUI; Bin PENG; Ming YAO.
Chinese Medical Journal ; (24): 178-184, 2020.
Artículo en Inglés | WPRIM | ID: wpr-877896

Documentos relacionados

  1. HTRA1-related autosomal dominant cerebral small vessel disease.
  2. Two Unique Mutations in HTRA1-Related Cerebral Small Vessel Disease in North America and Africa and Literature Review.
  3. Genotype-phenotype correlations of heterozygous HTRA1-related cerebral small vessel disease: case report and systematic review.
  4. Clinical features and pathogenicity assessment in patients with HTRA1-autosomal dominant disease.
  5. Characterization of Heterozygous <i>HTRA1</i> Mutations in Taiwanese Patients With Cerebral Small Vessel Disease.
  6. High frequency of <i>HTRA1</i> AND <i>ABCC6</i> mutations in Japanese patients with adult-onset cerebral small vessel disease.
  7. Hereditary cerebral small vessel disease: Assessment of a HTRA1 variant using protein stability predictors and 3D modelling.
  8. [Clinical practice recommendations for hereditary cerebral small vessel disease in China].
  9. Novel mutations in HTRA1-related cerebral small vessel disease and comparison with CADASIL.
  10. Report of two pedigrees with heterozygous HTRA1 variants-related cerebral small vessel disease and literature review.