C19orf12 and FA2H Mutations Are Rare in Italian Patients...

Seminars in Pediatric Neurology 2012 Vol. 19; Iss. 2

C19orf12 and FA2H Mutations Are Rare in Italian Patients With Neurodegeneration With Brain Iron Accumulation

Celeste Panteghini, Giovanna Zorzi, Paola Venco, Sabrina Dusi, Chiara Reale, Dario Brunetti, Luisa Chiapparini, Federica Zibordi, Brigitte Siegel, Barbara Garavaglia, Alessandro Simonati, Enrico Berti
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Volume:
19
Year:
2012
Language:
english
Pages:
1
DOI:
10.1016/j.spen.2012.03.006
File:
PDF, 1.75 MB
english, 2012
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