Detection of mutations m.3460G>A , m.11778G>A, m.14484T>C, m.14482C>G, m.14495A>G,m.14498T>C, m.14596A>T in the mitochondrial

Consult

Documentation:
Ref: LV0231 Categories: , , , , Diseases: Leber Hereditary Optic Neuropathy (LHON)Genes: MT-ATP6Delivery term: 28 days