Identification of novel mutations in the SLC25A15 Gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: A clinical, molecular, and functional study
Journal
Human Mutation
Journal Volume
30
Journal Issue
5
Pages
741-748
Date Issued
2009
Author(s)
Tessa A.
Fiermonte G.
Dionisi-Vici C.
Paradies E.
Baumgartner M.R.
Loguercio C.
De Baulny H.O.
Nassogne M.-C.
Schiff M.
Deodato F.
Parenti G.
Rutledge S.L.
Antonia Vilaseca M.
Melone M.A.B.
Scarano G.
Aldamiz-Echevarria L.
Besley G.
Walter J.
Martinez-Hernandez E.
Hernandez J.M.
Pierri C.L.
Palmieri F.
Santorelli F.M.
Type
journal article