Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation-Reference-Cited by-同舟云学术

Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation

Published:2023-05-22 Issue:10 Volume:8 Page:
ISSN:2379-3708
Container-title:JCI Insight
language:en
Short-container-title:

Author:

Lin Isabella^ORCID,Wei Angela^ORCID,Awamleh Zain,Singh Meghna^ORCID,Ning Aileen,Herrera Analeyla,Russell Bianca E.,Weksberg Rosanna,Arboleda Valerie A.^ORCID

Funder

NIH

ASXL Rare Research Endowment

Canadian Institutes of Health Research

Ontario Brain Institute

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Link

https://insight.jci.org/articles/view/167744/files/pdf

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