SA60 TRANSCRIPTIONAL CHANGES IN MOUSE MODELS OF THE 15Q13.3 MICRODELETION SYNDROME
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DOI: 10.1016/j.euroneuro.2017.08.132
Abstract: Background The 15q13.3 microdeletion syndrome is caused by a 1.5 MB hemizygous microdeletion at chromosome 15q13.3 affecting seven genes: FAN1, MTMR10, TRPM1, MIR211, KLF13, OTUD7A, and CHRNA7. The 15q13.3 microdeletion increases the risk of intellectual… read more here.
Keywords: 15q13 microdeletion; mouse models; microdeletion syndrome; microdeletion ... See more keywords