Showing results 1 to 4 of 4
Title | Author(s) | Issue Date | Views | |
---|---|---|---|---|
MECP2 mutation in male patients with non-specific X-linked mental retardation Journal:FEBS Letters | 2000 | |||
1999 | ||||
Resequencing the G6PT1 gene reveals a novel splicing mutation in a patient with glycogen storage disease type 1b Journal:Clinica Chimica Acta | 2006 | |||
A Rett syndrome MECP2 mutation that causes mental retardation in men Journal:Neurology | 2002 | 145 |