Ataxia, myoclonus, deafness, and neuropathy in a family carrying the mtDNA 11778/ND4 mutation previously associated with Leber's hereditary optic neuropathy

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作者：
Fulitano, Daniela
Goffredo, Castel
La Morgia, Chiara
Cantalupo, Gaetano
Achilli, Alessandro
Torroni, Antonio
Tonon, Caterina
Lodi, Raffaele
Liguori, Rocco
Valentino, Maria Lucia
Vetrugno, Roberto
Montagna, Pasquale
Baruzzi, Agostino
Martinelli, Paolo
Carelli, Valerio
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NEUROLOGY | 2008年 / 70卷 / 11期
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R74 [神经病学与精神病学];
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页码：A143 / A143
页数：1
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