A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspring
Por um escritor misterioso
Last updated 17 novembro 2024
A Novel Kleefstra Syndrome-associated Variant That Affects the
EHMT1 Gene - GeneCards, EHMT1 Protein
Using whole-exome sequencing to identify variants inherited from
Postzygotic single-nucleotide mosaicisms in whole-genome sequences
Short Report European Journal of Human Genetics
PDF) A de novo splice site mutation in EHMT1 resulting in
Aberrant splicing events caused by insertion of genes of interest
Hypogonadotropic Hypogonadism and Kleefstra Syndrome due to a
PDF) Cytogenetic and Molecular Genetic Characterization of
G9a and G9a-Like Histone Methyltransferases and Their Effect on
EHMT1 Gene - GeneCards, EHMT1 Protein
A mosaic maternal splice donor mutation in the EHMT1 gene leads to
PDF) EHMT1 mosaicism in apparently unaffected parents is
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