Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes. Linder MI, Mizoguchi Y, Hesse S, Csaba G, et al. Blood 2023;141:645-658.

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Amedeo Smart

Independent Medical Education

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Linder MI, Mizoguchi Y, Hesse S, Csaba G, et al. Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes. Blood 2023;141:645-658.
PMID: 36223592