Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease-Reference-Cited by-同舟云学术

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease

Published:2014-09-24 Issue:11 Volume:124 Page:4877-4881
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

French Curtis R.,Seshadri Sudha,Destefano Anita L.,Fornage Myriam,Arnold Corey R.,Gage Philip J.,Skarie Jonathan M.,Dobyns William B.,Millen Kathleen J.,Liu Ting,Dietz William,Kume Tsutomu,Hofker Marten,Emery Derek J.,Childs Sarah J.,Waskiewicz Andrew J.,Lehmann Ordan J.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference30 articles.

1. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

2. Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease

3. Role of COL4A1 in Small-Vessel Disease and Hemorrhagic Stroke

4. COL4A2 Mutations Impair COL4A1 and COL4A2 Secretion and Cause Hemorrhagic Stroke

5. Notch3 Mutations in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL), a Mendelian Condition Causing Stroke and Vascular Dementia

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