ZDHHC9

Publications

Baker K et al. Epilepsy, cognitive deficits and neuroanatomy in males with ZDHHC9 mutations. Ann Clin Transl Neurol. 2015;2(5):559-569. PMID: 26000327.

Han et al. The first patient with sporadic X-linked intellectual disability with de novo ZDHHC9 mutation identified by targeted next-generation sequencing. Europ J Med Genet. 2017;60(10): 499-503. PMID: 28687527.

Raymond FL et al. Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a marfanoid habitus. Am J Hum Genet. 2007;80(5):982-987. PMID: 17436253.

Schirwani S et al. Expanding the molecular basis and phenotypic spectrum of ZDHHC9-associated X-linked intellectual disability. Am J Med Genet A. 2018;176(5):1238-1244. PMID: 29681091.