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Clinical and molecular features of an infant patient affect..:
Moggio Maurizio
;
Capovilla Giuseppe
;
Cagdas Sophie
...
http://www.biomedcentral.com/1471-2377/11/85. , 2011
Link:
https://doi.org/10.1186/1471-2377-11-85
RT Journal T1
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G > A mitochondrial DNA mutation: a case report
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:3e81478040f2471a847c8fb3c49c64c7&Exemplar=1&LAN=DE A1 Moggio Maurizio A1 Capovilla Giuseppe A1 Cagdas Sophie A1 Collotta Martina A1 Sciacco Monica A1 Rizzuti Mafalda A1 Fortunato Francesco A1 Bordoni Andreina A1 Orcesi Simona A1 Tonduti Davide A1 Cosi Alessandra A1 Ronchi Dario A1 Berardinelli Angela A1 Veggiotti Pierangelo A1 Comi Giacomo P PB BMC YR 2011 K1 Leigh Syndrome K1 mitochondrial DNA K1 LHON K1 MT-ND6 K1 MT-CYB K1 mitochondrial Complex I K1 Neurology. Diseases of the nervous system K1 RC346-429 JF http://www.biomedcentral.com/1471-2377/11/85 LK http://dx.doi.org/https://doi.org/10.1186/1471-2377-11-85 DO https://doi.org/10.1186/1471-2377-11-85 SF ELIB - SuUB Bremen
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