PuSH - Publikationsserver des Helmholtz Zentrums München: Biallelic loss-of-function variants in RBL2 in siblings with a neurodevelopmental disorder.

Navigation

Startseite

English

Recherche

Erweiterte Suche

Durchblättern nach ...

... Zeitschriften

... Publikationstypen

... Forschungsdaten

... Erscheinungsjahr

Publikationen im Überblick

Hilfe & Kontakt

Ansprechpartner

Hilfe

Datenschutz

Brunet, T. ; Radivojkov-Blagojevic, M. ; Lichtner, P. ; Kraus, V.* ; Meitinger, T. ; Wagner, M.

Biallelic loss-of-function variants in RBL2 in siblings with a neurodevelopmental disorder.

Ann. Clin. Transl. Neurol. 7, 390-396 (2020)

Verlagsversion

Forschungsdaten

DOI

PMC

	Open Access Gold

Abstract
Metriken
Zusatzinfos

The RBL2 locus has been associated with intelligence and educational attainment but not with a monogenic disorder to date. RBL2 encodes p130, a member of the retinoblastoma protein family, which is involved in mediating neuron survival and death. Previous studies on p130 knockout mice revealing embryonic death and impaired neurogenesis underscore the importance of RBL2 in brain development. Exome sequencing in two siblings with severe intellectual disability, stereotypies and dysmorphic features identified biallelic loss-of-function variants c.556C>T, p.(Arg186Ter) and a deletion of exon 13-17 in RBL2 (NM_005611.3), establishing RBL2 as a candidate gene for an autosomal recessive neurodevelopmental disorder.

Altmetric

Weitere Metriken?

[➜Einloggen]