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Titel:

RPL26 variants: A rare cause of Diamond-Blackfan anemia syndrome with multiple congenital anomalies at the forefront.

Dokumenttyp:
Article; Journal Article
Autor(en):
Vanlerberghe, Clémence; Frénois, Frédéric; Smol, Thomas; Jourdain, Anne-Sophie; Escande, Fabienne; Aït-Yahya, Emilie; Aldeeri, Abdulrahman A; Yu, Timothy W; Cormier-Daire, Valérie; Ghoumid, Jamal; Jacob, Maureen; Newbury-Ecob, Ruth; Manouvrier, Sylvie; Platon, Jessica; Sailer, Sebastian; Brunelle, Perrine; Da Costa, Lydie; Petit, Florence
Abstract:
PURPOSE: Diamond-Blackfan anemia syndrome (DBS) is a rare congenital disorder originally characterized by bone marrow failure with or without various congenital anomalies. At least 24 genes are implicated, the vast majority encoding for ribosomal proteins. RPL26 (ribosomal protein L26) is an emerging candidate (DBA11, MIM#614900). We aim to further delineate this rare condition. METHODS: Patients carrying heterozygous RPL26 variants were recruited. In one of them, erythroid proliferation and dif...     »
Zeitschriftentitel:
Genet Med
Jahr:
2024
Band / Volume:
26
Heft / Issue:
12
Volltext / DOI:
doi:10.1016/j.gim.2024.101266
PubMed:
http://view.ncbi.nlm.nih.gov/pubmed/39268718
Print-ISSN:
1098-3600
TUM Einrichtung:
Institut für Humangenetik (Prof. Winkelmann)
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