Expanding the phenotype associated to KMT2A variants: overlapping
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Last updated 20 setembro 2024
PDF] KMT2A: Umbrella Gene for Multiple Diseases
Mutually suppressive roles of KMT2A and KDM5C in behaviour
Family A with KMT2A-associated Wiedemann-Steiner syndrome (WSS
Mutational spectrum and phenotypic variability of Duchenne
The social phenotype associated with Wiedemann‐Steiner syndrome
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PDF] KMT2A: Umbrella Gene for Multiple Diseases
Histone–lysine N-methyltransferase 2 (KMT2) complexes – a new
Frontiers Novel variants and phenotypic heterogeneity in a
Frontiers Genetic Mosaicism in a Group of Patients With Cornelia
Clinical and molecular spectrum of Wiedemann-Steiner syndrome, an
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PDF] KMT2A: Umbrella Gene for Multiple Diseases
Locations of ID/DD-associated KMT2A mutations. 22 mutations in
PDF) Clinical exome sequencing reveals locus heterogeneity and
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