Expanding the phenotype associated to KMT2A variants: overlapping
Por um escritor misterioso
Last updated 22 março 2025


Full article: Epigenetic regulation of autophagy-related genes

Molecular and cellular issues of KMT2A variants involved in

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Histone–lysine N-methyltransferase 2 (KMT2) complexes – a new

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Clinical and molecular spectrum of Wiedemann-Steiner syndrome, an

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Delineation of clinical features in Wiedemann – Steiner syndrome
RXRA DT448/9PP generates a dominant active variant capable of

Expanding the neurodevelopmental phenotypes of individuals with de

Analysis of KMT2A mutations in Wiedemann-Steiner syndrome vs ID/DD

Frontiers Novel variants and phenotypic heterogeneity in a
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