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Article

Immunoglobulin deficiency associated with a MAP2K1-related mutation causing cardio-facio-cutaneous syndrome.

Immunology letters - 1 Nov 2020

Leoni Chiara, Tedesco Marta, Onesimo Roberta, Giorgio Valentina, Rigante Donato, Zampino Giuseppe

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 32866538
DOI: 10.1016/j.imlet.2020.08.009

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Immunoglobulin deficiency associated with a MAP2K1-related mutation causing cardio-facio-cutaneous syndrome.PMID 32866538Read ↗

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Cutaneous IgA vasculitis-presenting manifestation of a novel mutation in the IKZF1 gene.Semantic proximity Read ↗

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Recurrent p.H119Y variant in MAP2K1 expands the phenotypic spectrum of MAP2K1 -related RASopathy.Semantic proximity Read ↗

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