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Genotype-phenotype correlations of heterozygous HTRA1-related cerebral small vessel disease: case report and systematic review.
Zhang, Haohan; Qin, Xiaoming; Shi, Yingying; Gao, Xinya; Wang, Fengyu; Wang, Huayuan; Shang, Junkui; Zhao, Jingyi; Zhang, Jiewen; Shao, Fengmin.
Afiliação
  • Zhang H; Department of Neurology, People's Hospital of Zhengzhou University, Henan Provincial People's Hospital, Zhengzhou, 450003, Henan, China.
  • Qin X; Department of Neurology, Fuwai Central China Cardiovascular Hospital, Zhengzhou, 450018, Henan, China.
  • Shi Y; Department of Neurology, People's Hospital of Zhengzhou University, Henan Provincial People's Hospital, Zhengzhou, 450003, Henan, China.
  • Gao X; Department of Neurology, People's Hospital of Zhengzhou University, Henan Provincial People's Hospital, Zhengzhou, 450003, Henan, China.
  • Wang F; Department of Neurology, People's Hospital of Zhengzhou University, Henan Provincial People's Hospital, Zhengzhou, 450003, Henan, China.
  • Wang H; Department of Neurology, People's Hospital of Zhengzhou University, Henan Provincial People's Hospital, Zhengzhou, 450003, Henan, China.
  • Shang J; Department of Neurology, People's Hospital of Zhengzhou University, Henan Provincial People's Hospital, Zhengzhou, 450003, Henan, China.
  • Zhao J; Department of Neurology, People's Hospital of Zhengzhou University, Henan Provincial People's Hospital, Zhengzhou, 450003, Henan, China.
  • Zhang J; Department of Neurology, People's Hospital of Zhengzhou University, Henan Provincial People's Hospital, Zhengzhou, 450003, Henan, China. zhangjiewen9900@126.com.
  • Shao F; Department of Nephrology, Henan Provincial Key Laboratory of Kidney Disease and Immunology, Zhengzhou University People's Hospital, Henan Provincial People's Hospital, Zhengzhou, 450003, Henan, China. fengminshao@126.com.
Neurogenetics ; 22(3): 187-194, 2021 07.
Article em En | MEDLINE | ID: mdl-33963955
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Doenças da Coluna Vertebral / Infarto Cerebral / Alopecia / Leucoencefalopatias / Serina Peptidase 1 de Requerimento de Alta Temperatura A / Mutação Tipo de estudo: Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Adult / Humans / Male / Middle aged Idioma: En Revista: Neurogenetics Assunto da revista: GENETICA / NEUROLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Doenças da Coluna Vertebral / Infarto Cerebral / Alopecia / Leucoencefalopatias / Serina Peptidase 1 de Requerimento de Alta Temperatura A / Mutação Tipo de estudo: Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Adult / Humans / Male / Middle aged Idioma: En Revista: Neurogenetics Assunto da revista: GENETICA / NEUROLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China