Cite
MLA Citation
Mylène Tharreau et al.. “Refining the clinical phenotype associated with missense variants in exons 38 and 39 of KMT2D.” American journal of medical genetics, vol. 188, no. 5, 2022, pp. 1600–1606. http://access.bl.uk/ark:/81055/vdc_100153439631.0x000009