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Title:

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.

Document type:
Published Erratum
Author(s):
Paul, Maimuna S; Duncan, Anna R; Genetti, Casie A; Pan, Hongling; Jackson, Adam; Grant, Patricia E; Shi, Jiahai; Pinelli, Michele; Brunetti-Pierri, Nicola; Garza-Flores, Alexandra; Shahani, Dave; Saneto, Russell P; Zampino, Giuseppe; Leoni, Chiara; Agolini, Emanuele; Novelli, Antonio; Blümlein Tobias B Haack, Ulrike; Heinritz, Wolfram; Matzker, Eva; Alhaddad, Bader; Jamra, Rami Abou; Bartolomaeus, Tobias; AlHamdan, Saber; Carapito, Raphael; Isidor, Bertrand; Bahram, Seiamak; Ritter, Alyssa; Izum...     »
Journal title abbreviation:
Am J Hum Genet
Year:
2023
Journal volume:
110
Journal issue:
3
Fulltext / DOI:
doi:10.1016/j.ajhg.2023.02.010
Pubmed ID:
http://view.ncbi.nlm.nih.gov/pubmed/36868207
Print-ISSN:
0002-9297
TUM Institution:
Institut für Humangenetik (Prof. Winkelmann)
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