Document is current

Any future updates will be listed below

De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing

Crossref DOI link: https://doi.org/10.1186/1471-2350-15-49

Published Online: 2014-05-01

Published Print: 2014-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

About CrossMark