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American Journal of Human Genetics|June 23, 2023
Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humansLong Guo, Smrithi Salian, Jing-Yi Xue, et al.EMBO Molecular Medicine|November 9, 2021
Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypesSilvia Vidali, Raffaele Gerlini, Kyle Thompson, et al.Nature Communications|March 15, 2022
The arginine methyltransferase PRMT7 promotes extravasation of monocytes resulting in tissue injury in COPDGizem Günes Günsel, Thomas M Conlon, Aicha Jeridi, et al.Pageof 8