- Title
- Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
- Creators
- Janel O JohnsonJessica MandrioliMichael BenatarYevgeniya AbramzonVivianna M Van DeerlinJohn Q TrojanowskiJ. Raphael GibbsMaura BrunettiSusan GronkaJoanne WuuJinhui DingLeo McCluskeyMaria Martinez-LageDana FalconeDena G HernandezSampath ArepalliSean ChongJennifer C SchymickJeffrey RothsteinFrancesco LandiYong-Dong WangAndrea CalvoGabriele MoraMario SabatelliMaria Rosaria MonsurròStefania BattistiniFabrizio SalviRossella SpataroPatrizia SolaGiuseppe BorgheroGiuliana GalassiSonja W ScholzJ. Paul TaylorGabriella RestagnoAdriano ChiòBryan J TraynorThe ITALSGEN Consortium
- Publication Details
- Neuron (Cambridge, Mass.), Vol.69(2), pp.397-397
- Academic Unit
- Miller School of Medicine; UMMG Department of Neurology; UMMG Dept of Neurology - Neuromuscular Disorders Div
- Language
- English
- Resource Type
- Journal article
- Record Identifier
- 991031600554502976
Journal article
Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
Neuron (Cambridge, Mass.), Vol.69(2), pp.397-397
2011-01
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- Citation topics
- 1 Clinical & Life Sciences
- 1.52 Neurodegenerative Diseases
- 1.52.765 Amyotrophic Lateral Sclerosis
- Web Of Science research areas
- Neurosciences
- ESI research areas
- Neuroscience & Behavior
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Source: InCites