Publication | Open Access
Expanding the PRAAS spectrum: De novo mutations of immunoproteasome subunit β-type 10 in six infants with SCID-Omenn syndrome
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Citations
44
References
2024
Year
Genetic DisorderMedicineImmunodeficienciesGeneticsImmunologyPathogenesisPathologyScid-omenn SyndromeInborn Error Of ImmunityDisease Gene IdentificationMolecular DiagnosticsPraas Spectrum
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