CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy-Reference-Cited by-同舟云学术

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CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy

Published:2017-03 Issue:3 Volume:100 Page:488-505
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Barbé Lise,Lanni Stella,López-Castel Arturo,Franck Silvie,Spits Claudia,Keymolen Kathelijn,Seneca Sara,Tomé Stephanie,Miron Ioana,Letourneau Julie,Liang Minggao,Choufani Sanaa,Weksberg Rosanna,Wilson Michael D.,Sedlacek Zdenek,Gagnon Cynthia,Musova Zuzana,Chitayat David,Shannon Patrick,Mathieu Jean,Sermon Karen,Pearson Christopher E.

Funder

Canadian Institutes of Health Research

Muscular Dystrophy Canada

Tribute Communities

Kazman Family Fund

The Marigold Foundation

Petroff Family

Fonds voor Wetenschappelijk Onderzoek-Vlaanderen

Leerstoel Mireille Aerens

Methusalem

Association Belge contre les Maladies neuro-Musculaires fund

Canada Research Chair

Hospital for Sick Children Foundation Student Scholarship Program

NSERC

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference111 articles.

1. Disease-associated repeat instability and mismatch repair;Schmidt;DNA Repair (Amst.),2016

2. Anticipation in myotonic dystrophy. I. Statistical verification based on clinical and haplotype findings;Ashizawa;Neurology,1992

3. Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat;Ashizawa;Neurology,1992

4. Congenital and infantile myotonic dystrophy;Echenne;Handb. Clin. Neurol.,2013

5. Autism spectrum conditions in myotonic dystrophy type 1: a study on 57 individuals with congenital and childhood forms;Ekström;Am. J. Med. Genet. B. Neuropsychiatr. Genet.,2008

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