WNT1-associated osteogenesis imperfecta with atrophic frontal lobes and arachnoid cysts

WNT1-associated osteogenesis imperfecta with atrophic frontal lobes and arachnoid cysts

© 2019, The Author(s) under exclusive licence to The Japan Society of Human Genetics. A rare form of osteogenesis imperfecta (OI) caused by Wingless-type MMTV integration site family 1 (WNT1) mutations combines central nervous system (CNS) anomalies with the characteristic increased susceptibility t...

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Bibliographic Details
Main Authors: Piranit Nik Kantaputra, Yuddhasert Sirirungruangsarn, Pannee Visrutaratna, Sasitorn Petcharunpaisan, Bruce M. Carlson, Worrachet Intachai, Jutamas Sudasna, Jatupol Kampuansai, Prapai Dejkhamron
Format: Journal
Published: 2019
Subjects:
Biochemistry, Genetics and Molecular Biology
Medicine
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85060775236&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/63570
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Institution: Chiang Mai University

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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85060775236&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/63570

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