Potassium

lysine methyltransferase 2D ; Homo sapiens







3 Article(s)
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PMID
Title
Pub. Year
#Total Relationships
1 33334222 Ocular manifestations in kabuki syndrome: A report of 10 cases and literature review. 2021 Apr 1
2 31446696 [One novel pathologic variation in KMT2D cause Kabuki syndrome with hearing loss as the main phenotype and related research on types of deafness]. 2019 Sep 1
3 30107592 Dissecting KMT2D missense mutations in Kabuki syndrome patients. 2018 Nov 1 2