Title : RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome.

Pub. Date : 2015 Sep

PMID : 26280580






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Dominant mutations in the chromatin regulators lysine (K)-specific methyltransferase 2D (KMT2D) (also known as MLL2) and lysine (K)-specific demethylase 6A (KDM6A) underlie the majority of cases. Lysine lysine methyltransferase 2D Homo sapiens
2 Dominant mutations in the chromatin regulators lysine (K)-specific methyltransferase 2D (KMT2D) (also known as MLL2) and lysine (K)-specific demethylase 6A (KDM6A) underlie the majority of cases. Lysine lysine methyltransferase 2D Homo sapiens