Mitochondrial DNA point mutation G11778A is associated with Leber's hereditary optic neuroretinopathy (LHON) in two Croatian families (CROSBI ID 521437)
Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija
Podaci o odgovornosti
Martin-Kleiner, Irena ; Gabrilovac, Jelka ; Bradvica, Mario ; Vidović, Tomislav ; Cerovski, Branimir ; Fumić, Ksenija ; Čupić, Barbara ; Boranić, Milivoj
engleski
Mitochondrial DNA point mutation G11778A is associated with Leber's hereditary optic neuroretinopathy (LHON) in two Croatian families
LHON G11778A mitochondrial DNA point mutations were tested in five Croatian families with members having severe visual impairment. The mutation was detected in 10 of 24 tested individuals in two families.
LHON; visual impairment; mitochondrial DNA; G11778A point mutation
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
Podaci o prilogu
69-69-x.
2006.
objavljeno
Podaci o matičnoj publikaciji
EMBO/HHMI Central European Scientists Meeting 2006, Conference Proceedings
.
HHMI - Howard Hughes Medical Institute
Podaci o skupu
EMBO/HHMI Central European Scientists Meeting 2006
poster
15.06.2006-17.06.2006
Cavtat, Hrvatska
