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ArticleClinical case reports2022

Expanding the phenotype of the recurrent truncating eIF2γ pathogenic variant p.(Ile465Serfs*4) identified in two brothers with MEHMO syndrome.

Sofia Ygberg et al.PubMed ↗Full text ↗Publisher ↗

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2022
2023
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Full record →Abstract, authors, funding and every citing paper · PMID 35765291