[HTML][HTML] A functional mini-GDE transgene corrects impairment in models of glycogen storage disease type III
A Gardin, J Rouillon… - The Journal of …, 2024 - Am Soc Clin Investig
Glycogen storage disease type III (GSDIII) is a rare inborn error of metabolism affecting liver,
skeletal muscle, and heart due to mutations of the AGL gene encoding for the glycogen …
skeletal muscle, and heart due to mutations of the AGL gene encoding for the glycogen …
A functional mini-GDE transgene corrects impairment in models of glycogen storage disease type III.
A Gardin, J Rouillon, V Montalvo-Romeral… - The Journal of …, 2024 - europepmc.org
Glycogen storage disease type III (GSDIII) is a rare inborn error of metabolism affecting liver,
skeletal muscle, and heart due to mutations of the AGL gene encoding for the glycogen …
skeletal muscle, and heart due to mutations of the AGL gene encoding for the glycogen …
[HTML][HTML] A functional mini-GDE transgene corrects impairment in models of glycogen storage disease type III
A Gardin, J Rouillon, V Montalvo-Romeral… - The Journal of …, 2024 - ncbi.nlm.nih.gov
Glycogen storage disease type III (GSDIII) is a rare inborn error of metabolism affecting liver,
skeletal muscle, and heart due to mutations of the AGL gene encoding for the glycogen …
skeletal muscle, and heart due to mutations of the AGL gene encoding for the glycogen …
[引用][C] A functional mini-GDE transgene corrects impairment in models of glycogen storage disease type III
A Gardin, J Rouillon… - The Journal of …, 2023 - univ-evry.hal.science
A functional mini-GDE transgene corrects impairment in models of glycogen storage disease
type III - Université d'Évry Access content directly Documentation EN English (EN) French (FR) …
type III - Université d'Évry Access content directly Documentation EN English (EN) French (FR) …
A functional mini-GDE transgene corrects impairment in models of glycogen storage disease type III
A Gardin, J Rouillon… - The Journal of …, 2024 - pubmed.ncbi.nlm.nih.gov
Glycogen storage disease type III (GSDIII) is a rare inborn error of metabolism affecting liver,
skeletal muscle, and heart due to mutations of the AGL gene encoding for the glycogen …
skeletal muscle, and heart due to mutations of the AGL gene encoding for the glycogen …
A functional mini-GDE transgene corrects impairment in models of glycogen storage disease type III.
A Gardin, J Rouillon, V Montalvo-Romeral… - Journal of Clinical …, 2024 - go.gale.com
Glycogen storage disease type III (GSDIII) is a rare inborn error of metabolism affecting liver,
skeletal muscle, and heart due to mutations of the AGL gene encoding for the glycogen …
skeletal muscle, and heart due to mutations of the AGL gene encoding for the glycogen …
[引用][C] A functional mini-GDE transgene corrects impairment in models of glycogen storage disease type III
A Gardin, J Rouillon, V Montalvo-Romeral… - The Journal of clinical …, 2023 - hal.science
A functional mini-GDE transgene corrects impairment in models of glycogen storage disease
type III - Archive ouverte HAL Accéder directement au contenu Documentation FR Français …
type III - Archive ouverte HAL Accéder directement au contenu Documentation FR Français …
A functional mini-GDE transgene corrects impairment in models of glycogen storage disease type III.
A Gardin, J Rouillon, V Montalvo-Romeral… - The Journal of …, 2023 - europepmc.org
Glycogen storage disease type III (GSDIII) is a rare inborn error of metabolism affecting liver,
skeletal muscle, and heart due to mutations of the AGL gene encoding for the glycogen …
skeletal muscle, and heart due to mutations of the AGL gene encoding for the glycogen …