Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.
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Linder MI, et al. Among authors: schwestka m.
Blood. 2023 Feb 9;141(6):645-658. doi: 10.1182/blood.2022016783.
Blood. 2023.
PMID: 36223592
Free PMC article.