Title : Kabuki syndrome: review of the clinical features, diagnosis and epigenetic mechanisms.

Pub. Date : 2019 Dec

PMID : 31587141






4 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 BACKGROUND: Kabuki syndrome (KS), is a infrequent inherited malformation syndrome caused by mutations in a H3 lysine 4 methylase (KMT2D) or an X-linked histone H3 lysine 27 demethylase (UTX/KDM6A). Lysine lysine demethylase 6A Homo sapiens
2 BACKGROUND: Kabuki syndrome (KS), is a infrequent inherited malformation syndrome caused by mutations in a H3 lysine 4 methylase (KMT2D) or an X-linked histone H3 lysine 27 demethylase (UTX/KDM6A). Lysine lysine demethylase 6A Homo sapiens
3 BACKGROUND: Kabuki syndrome (KS), is a infrequent inherited malformation syndrome caused by mutations in a H3 lysine 4 methylase (KMT2D) or an X-linked histone H3 lysine 27 demethylase (UTX/KDM6A). Lysine lysine demethylase 6A Homo sapiens
4 BACKGROUND: Kabuki syndrome (KS), is a infrequent inherited malformation syndrome caused by mutations in a H3 lysine 4 methylase (KMT2D) or an X-linked histone H3 lysine 27 demethylase (UTX/KDM6A). Lysine lysine demethylase 6A Homo sapiens