A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease - Concepedia

Concepedia

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A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

529

Citations

4

References

2005

Year

Alessio Di Fonzo, Christan F. Rohé, Joaquim J. Ferreira, Hsin Fen Chien, Laura Vacca, Fabrizio Stocchi, Leonor Correia Guedes, Edito Fabrizio, M. Manfredi, Nicola Vanacore,

Molecular NeuroscienceMendelian DisorderAutosomal Dominant ParkinsonGenetic DisorderParkinson DiseaseGeneticsPathologyDisease Gene IdentificationMedicineNeurogenetics

References

	Year	Citations

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