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

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

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