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Cutting edge: a hypomorphic mutation in Ig (CD79b) in a patient with immunodeficiency and a leaky defect in B cell development

doi: 10.1016/j.ramb.2013.03.003 107 Begin-HeickNDalpe-ScottMRoweJHeickHM

Its broad activity across multiple tissue types an unusual characteristic for a single peptide compound has been a recurring focus of mechanistic discussion in the research literature, with studies examining growth hormone receptor upregulation as a potential unifying mechanism

[DOI] [PMC free article] [PubMed] [Google Scholar] 43.Ito Y, Miyauchi A, Fujishima M, Noda T, Sano T, et al

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Patterns and rates of exonic de novo mutations in autism spectrum disorders