Leber’s hereditary optic neuropathy, intellectual disability and epilepsy presenting with variable penetrance associated to the m.3460G >A mutation and a heteroplasmic expansion of the microsatellite in MTRNR1 gene – case report
2017 ◽
Vol 38
(12)
◽
pp. 2213-2215
◽
2017 ◽
Vol 23
(2)
◽
pp. 165-168
2011 ◽
Vol 51
(10)
◽
pp. 781-783
◽
2020 ◽
pp. 101-102
2003 ◽
Vol 19
(10)
◽
pp. 516-520
◽
2004 ◽
Vol 122
(6)
◽
pp. 276-279
◽
2018 ◽
Vol 62
(1)
◽
pp. 64-71
◽