Inherited human Apollo deficiency causes severe bone marrow failure and developmental defects

Inherited bone marrow failure syndromes (IBMFSs) are a group of disorders typified by impaired production of 1 or several blood cell types. The telomere biology disorders dyskeratosis congenita (DC) and its severe variant, Høyeraal-Hreidarsson (HH) syndrome, are rare IBMFSs characterized by bone mar...

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Main Authors: Abdo, C. (Author), Audebert-Bellanger, S. (Author), Awad, A. (Author), Bottero, A. (Author), Callebaut, I. (Author), Churikov, D. (Author), Costa, E. (Author), Danielian, S. (Author), de Villartay, J.-P (Author), Géli, V. (Author), Haro, S. (Author), Kannengiesser, C. (Author), Kermasson, L. (Author), Lainey, E. (Author), Mouf, M. (Author), Oleastro, M. (Author), Revy, P. (Author), Roger, L. (Author), Smoom, R. (Author), Soares, G. (Author), Touzot, F. (Author), Tzfati, Y. (Author)
Format: Article
Language:English
Published: NLM (Medline) 2022
Online Access:View Fulltext in Publisher