Title : [One novel pathologic variation in KMT2D cause Kabuki syndrome with hearing loss as the main phenotype and related research on types of deafness].

Pub. Date : 2019 Sep

PMID : 31446696






1 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 KMT2D and KDM6A are two pathogenic genes that have been identified for KS. Potassium lysine methyltransferase 2D Homo sapiens