A Swedish family with de novo α-synuclein A53T mutation: Evidence for early cortical dysfunction - Concepedia

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A Swedish family with de novo α-synuclein A53T mutation: Evidence for early cortical dysfunction

DOI Full Paper Access

99

Citations

21

References

2009

Year

Andreas Puschmann, Owen A. Ross, Carles Vilariño‐Güell, Sarah Lincoln, Jennifer M. Kachergus, Stephanie A. Cobb, Suzanne Granhøj Lindquist, Jørgen E. Nielsen, Zbigniew K. Wszołek, Matthew J. Farrer,

Parkinsonism & Related Disorders

Neurodegenerative DiseasesNeurobiology Of DiseaseMolecular NeuroscienceMendelian DisorderGeneticsSwedish Familyα-Synuclein A53t MutationDegenerative DiseaseDegenerative PathologyEarly Cortical DysfunctionNeurologyNeuroscienceNeurodegenerationNeuropathologyMedicineSocial SciencesNeurogenetics

References

	Year	Citations

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