Biallelic loss‐of‐function variants inRBL2in siblings with a neurodevelopmental disorder-Reference-Cited by-同舟云学术

Biallelic loss‐of‐function variants inRBL2in siblings with a neurodevelopmental disorder

Published:2020-03 Issue:3 Volume:7 Page:390-396
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Brunet Theresa¹²^ORCID,Radivojkov‐Blagojevic Milena²,Lichtner Peter²,Kraus Verena³,Meitinger Thomas¹²,Wagner Matias¹²⁴

Affiliation:

1. Institute of Human Genetics, Faculty of Medicine Technical University Munich Munich Germany

2. Institute of Human Genetics Helmholtz Zentrum München Neuherberg Germany

3. Department of Pediatrics Klinik für Kinder‐ und JugendmedizinMünchen Klinik Schwabing und HarlachingKlinikum Rechts der Isar der Technischen Universität Munich Munich Germany

4. Institute for Neurogenomics Helmholtz Zentrum München Neuherberg Germany

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.50992

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4. RBL2/p130: a direct AKT substrate and mediator of AKT inhibition‐induced apoptosis;Ventura E;Oncoscience,2018

5. Nucleocytoplasmic Shuttling of p130/RBL2: Novel Regulatory Mechanism

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