Multi-infarct dementia of Swedish type is caused by a 3’UTR mutation of COL4A1-Reference-Cited by-同舟云学术

Multi-infarct dementia of Swedish type is caused by a 3’UTR mutation of COL4A1

Published:2017-03-28 Issue:5 Volume:140 Page:e29-e29
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:

Author:

Siitonen Maija,Börjesson-Hanson Anne,Pöyhönen Minna,Ora Ari,Pasanen Petra,Bras Jose,Kern Silke,Kern Jürgen,Andersen Oluf,Stanescu Horia,Kleta Robert,Baumann Marc,Kalaria Rajesh,Kalimo Hannu,Singleton Andy,Hardy John,Viitanen Matti,Myllykangas Liisa,Guerreiro Rita

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/140/5/e29/18223894/awx062.pdf

Reference15 articles.

1. Quantitative vascular pathology and phenotyping familial and sporadic cerebral small vessel diseases;Brain Pathol,2013

2. A framework for variation discovery and genotyping using next-generation DNA sequencing data;Nat Genet,2011

3. Allegro, a new computer program for multipoint linkage analysis;Nat Genet,2000

4. Subcortical angiopathic encephalopathy in a German kindred suggests an autosomal dominant disorder distinct from CADASIL;Acta Neuropathol,2004

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