Browsing by Subject "Dwarfism"
Now showing items 1-1 of 1
-
(2015-07-17)Department: PharmacologyNeurofibromatosis type 1 (NF1) is the most common autosomal dominant genetic disorder occurring in 1 of every 3500 live births. NF1 is caused by loss-of-function mutations in NF1, the gene encoding the Ras-GAP neurofibromin. ...