1-1 of 1
Keywords: PCH2a
Close
Save search
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Journal Articles

Human organoid model of pontocerebellar hypoplasia 2a recapitulates brain region-specific size differences

Open Access
In collection:
Advanced in vitro models , Rare Disease Translational Research , Review Commons Transfers
Theresa Kagermeier, Stefan Hauser, Kseniia Sarieva, Lucia Laugwitz, Samuel Groeschel, Wibke G. Janzarik, Zeynep Yentür, Katharina Becker, Ludger Schöls, Ingeborg Krägeloh-Mann, Simone Mayer
Journal: Disease Models & Mechanisms
Series: REVIEW COMMONS TRANSFER
Dis Model Mech (2024) 17 (7): dmm050740.
https://doi.org/10.1242/dmm.050740
Published: 22 July 2024
...Theresa Kagermeier; Stefan Hauser; Kseniia Sarieva; Lucia Laugwitz; Samuel Groeschel; Wibke G. Janzarik; Zeynep Yentür; Katharina Becker; Ludger Schöls; Ingeborg Krägeloh-Mann; Simone Mayer ABSTRACT Pontocerebellar hypoplasia type 2a (PCH2a) is an ultra-rare, autosomal recessive pediatric disorder...
View article titled, Human organoid model of pontocerebellar hypoplasia 2a recapitulates brain region-specific size differences
Open the PDF for Human organoid model of pontocerebellar hypoplasia 2a recapitulates brain region-specific size differences in another window
Includes: Supplementary data