Intrinsic link between PGRN and Gba1 D409V mutation dosage in potentiating Gaucher disease

Y Lin, X Zhao, B Liou, V Fannin, W Zhang… - Human Molecular …, 2024 - academic.oup.com
Gaucher disease (GD) is caused by biallelic GBA1/Gba1 mutations that encode defective
glucocerebrosidase (GCase). Progranulin (PGRN, encoded by GRN/Grn) is a modifier of …
相关文章

Intrinsic link between PGRN and Gba1 D409V mutation dosage in potentiating Gaucher disease

Y Lin, X Zhao, B Liou, V Fannin, W Zhang… - Human Molecular …, 2024 - academic.oup.com
Gaucher disease (GD) is caused by biallelic GBA1/Gba1 mutations that encode defective
glucocerebrosidase (GCase). Progranulin (PGRN, encoded by GRN/Grn) is a modifier of …

Intrinsic link between PGRN and Gba1 D409V mutation dosage in potentiating Gaucher disease

Y Lin, X Zhao, B Liou, V Fannin… - Human molecular …, 2024 - pubmed.ncbi.nlm.nih.gov
Gaucher disease (GD) is caused by biallelic GBA1/Gba1 mutations that encode defective
glucocerebrosidase (GCase). Progranulin (PGRN, encoded by GRN/Grn) is a modifier of …
[PDF] researchgate.net

[PDF][PDF] Intrinsic link between PGRN and Gba1 D409V mutation dosage in potentiating Gaucher disease

Y Lin, X Zhao, B Liou, V Fannin, W Zhang… - Human Molecular …, 2024 - researchgate.net
Gaucher disease (GD) is caused by biallelic GBA1/Gba1 mutations that encode defective
glucocerebrosidase (GCase). Progranulin (PGRN, encoded by GRN/Grn) is a modifier of …

Intrinsic link between PGRN and Gba1 D409V mutation dosage in potentiating Gaucher disease.

Y Lin, X Zhao, B Liou, V Fannin, W Zhang… - Human Molecular …, 2024 - europepmc.org
Gaucher disease (GD) is caused by biallelic GBA1/Gba1 mutations that encode defective
glucocerebrosidase (GCase). Progranulin (PGRN, encoded by GRN/Grn) is a modifier of …