A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion

Chai, G., Szenker-Ravi, E., Chung, C., Li, Z., Wang, L., Khatoo, M., Marshall, T., Jiang, N., Yang, X., McEvoy-Venneri, J., Stanley, V., Anzenberg, P., Lang, N., Wazny, V., Yu, J., Virshup, D. M., Nygaard, R., Mancia, F., Merdzanic, R., … Gleeson, J. G. (2021). A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion. New England Journal of Medicine, 385(14), 1292–1301. https://doi.org/10.1056/nejmoa2033911
Authors:
Guoliang Chai
Emmanuelle Szenker-Ravi
Changuk Chung
Zhen Li
Lu Wang
Muznah Khatoo
Trevor Marshall
Nan Jiang
Xiaoxu Yang
Jennifer McEvoy-Venneri
Valentina Stanley
Paula Anzenberg
Nhi Lang
Vanessa Wazny
Jia Yu
David M Virshup
Rie Nygaard
Filippo Mancia
Rijad Merdzanic
Maria B P Toralles
Paula M L Pitanga
Ratna D Puri
Rebecca Hernan
Wendy K Chung
Aida M Bertoli-Avella
Nouriya Al-Sannaa
Maha S Zaki
Karl Willert
Bruno Reversade
Joseph G Gleeson
Affiliated Authors:
Guoliang Chai
Emmanuelle Szenker-Ravi
Changuk Chung
Zhen Li
Lu Wang
Muznah Khatoo
Trevor Marshall
Nan Jiang
Xiaoxu Yang
Jennifer McEvoy-Venneri
Valentina Stanley
Paula Anzenberg
Nhi Lang
Vanessa Wazny
Jia Yu
David M Virshup
Rie Nygaard
Filippo Mancia
Rijad Merdzanic
Maria B P Toralles
Paula M L Pitanga
Ratna D Puri
Rebecca Hernan
Wendy K Chung
Aida M Bertoli-Avella
Nouriya Al-Sannaa
Maha S Zaki
Karl Willert
Bruno Reversade
Joseph G Gleeson
Columbia Affiliation:
Subjects:
Abnormalities, Multiple (MeSH)
Congenital Abnormalities (MeSH)
Genetic Pleiotropy (MeSH)
Intracellular Signaling Peptides and Proteins (MeSH)
Mutation (MeSH)
Receptors, G-Protein-Coupled (MeSH)
Wnt Proteins (MeSH)
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Publication Type:
Article
Unique ID:
10.1056/nejmoa2033911
PMID:
34587386
DOI:
10.1056/nejmoa2033911
Journal:
New England Journal of Medicine
Publication Date:
Data Source:
PubMed
Source Link:
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Record Created: