MED12 Mutation in Two Families with X-Linked Ohdo Syndrome.
Rocchetti L, Evangelista E, De Falco L, Savarese G, Savarese P, Ruggiero R, D'Amore L, Sensi A, Fico A.
Rocchetti L, et al. Among authors: de falco l.
Genes (Basel). 2021 Aug 27;12(9):1328. doi: 10.3390/genes12091328.
Genes (Basel). 2021.
PMID: 34573309
Free PMC article.