Associated Papers
Complement cascade functions during brain development and neurodegeneration.
Fatoba O et al.
The Febs Journal, 2022
Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients.
Phetthong T et al.
Orphanet Journal of Rare Diseases, 2021
Three mutations of adult type 1 Gaucher disease found in a Chinese patient: A case report.
Du X et al.
Medicine, 2018
A common and two novel GBA mutations in Thai patients with Gaucher disease.
Tammachote R et al.
Journal of Human Genetics, 2013
Select a paper to view details