Reply to: "Differences in Sex-Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism"

Mov Disord. 2023 Apr;38(4):712-713. doi: 10.1002/mds.29351.

Authors

Nikola Kresojević^{1

2}, Vladana Marković^{1

2}, Valerija Dobričić^{1

3}, Iva Stanković^{1

2}, Tanja Stojković^{1

2}, Aleksandra Tomić^{1

2}, MIlica Ječmenica Lukić^{1

2}, Milena Janković¹, Ana Marjanović¹, Marija Branković¹, Ivana Novaković², Igor Petrović^{1

2}, Nataša Dragašević^{1

2}, Marina Svetel^{1

2}, Vladimir Kostić^{1

2}

Affiliations

¹ Neurology Clinic, University Clinical Center of Serbia, Belgrade, Serbia.
² Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
³ Lübeck Interdisciplinary Platform for Genome Analytics, University of Lübeck, Lübeck, Germany.

PMID: 37061878
DOI: 10.1002/mds.29351

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't
Comment

MeSH terms

Female
Gaucher Disease*
Glucosylceramidase / genetics
Heterozygote
Humans
Male
Mutation / genetics
Parkinsonian Disorders* / genetics

Substances

Glucosylceramidase