Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability.
Journal Information
Full Title: Neurogenetics
Abbreviation: Neurogenetics
Country: Unknown
Publisher: Unknown
Language: N/A
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"Disclosure All experiments comply with the current laws of the country in which they were performed. The authors declare that they have no conflict of interest."
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Evidence found in paper:
"This study was supported by a grant from the Internationaal Parkinson Fonds (The Netherlands) to Dr. Bonifati. We thank all the family members for their participation and Tom de Vries-Lentsch (Department of Clinical Genetics, Erasmus MC) for the artwork."
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Last Updated: Aug 05, 2025