Published in
BioMed Central, BMC Medical Genetics, 1(19), 2018
DOI: 10.1186/s12881-018-0644-3
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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
Journal article published in 2018 by
Angelica Bianco,
Luigi Bisceglia,
Maria Fara De Caro,
Valeria Galeandro,
Patrizia De Bonis,
Apollonia Tullo,
Stefano Zoccolella,
Silvana Guerriero 
,
Vittoria Petruzzella
,
Vittoria Petruzzella
This paper is made freely available by the publisher.
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