MUTATIONS IN MYO9B ARE ASSOCIATED WITH CMT2 NEUROPATHIES AND ISOLATED OPTIC ATROPHY

被引:0
作者
Bolino, Alessandra [1 ]
Cipriani, Silvia [1 ]
Guerrero-Valero, Marta [1 ]
Tozza, Stefano [2 ]
Vollmer, Veith [3 ]
Beijer, Danique [4 ,5 ]
Danzi, Matt [4 ,5 ]
Rivellini, Cristina [1 ]
Pipitone, Giovanni Battista [1 ]
Grosz, Bianca Rose [6 ,7 ]
Lamperti, Costanza [8 ]
Marzoli, Stefania Bianchi [9 ]
Carrera, Paola [1 ]
Devoto, Marcella [10 ]
Pisciotta, Chiara
Pareyson, Davide [11 ]
Kennerson, Marina [6 ,7 ]
Previtali, Stefano Carlo [12 ]
Zuchner, Stephan [4 ,5 ]
Scherer, Steven [13 ]
Manganelli, Fiore
Baehler, Martin [3 ]
机构
[1] IRCCS Hosp San Raffaele, Div Neurosci, Milan, Italy
[2] Univ Naples Federico II, Dept Neurosci Reprod Sci & Odontostomatol, Naples, Italy
[3] Westfalian Wilhelms Univ Munster, Inst Integrat Cell Biol & Physiol, Munster, Germany
[4] Univ Miami, Dept Human Genet, Miami, FL USA
[5] Hussman Inst Human Gen, Miami, FL USA
[6] Univ Sydney, ANZAC Res Inst Sydney Local Hlth Dist, Sydney, NSW, Australia
[7] Fac Hlth & Med, Sydney, NSW, Australia
[8] IRCCS Fdn Carlo Besta Neurol Inst, Genet & Neurogenet Unit, Milan, Italy
[9] Capitanio Hosp, Sci Inst Auxol, Dept Ophthalmol, Milan, Italy
[10] Inst Genet & Biomed Res IRGB, Cagliari, Italy
[11] IRCCS Fdn Carlo Besta Neurol Inst, Dept Clin Neurosci, Unit Rare Neurodegenerat & Neurometabol Dis, Milan, Italy
[12] IRCCS Hosp San Raffaele, Dept Neurol, Milan, Italy
[13] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
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R74 [神经病学与精神病学];
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页码:S10 / S10
页数:1
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