Modeling Phenotypic Heterogeneity of Glycogen Storage Disease Type 1a Liver Disease in Mice by Somatic CRISPR/CRISPR‐associated protein 9–Mediated Gene Editing-Reference-Cited by-同舟云学术

Modeling Phenotypic Heterogeneity of Glycogen Storage Disease Type 1a Liver Disease in Mice by Somatic CRISPR/CRISPR‐associated protein 9–Mediated Gene Editing

Published:2021-08-15 Issue:5 Volume:74 Page:2491-2507
ISSN:0270-9139
Container-title:Hepatology
language:en
Short-container-title:Hepatology

Author:

Rutten Martijn G.S.¹^ORCID,Derks Terry G.J.²^ORCID,Huijkman Nicolette C.A.¹,Bos Trijnie³,Kloosterhuis Niels J.¹,Kolk Kees C.W.A.⁴,Wolters Justina C.¹^ORCID,Koster Mirjam H.¹^ORCID,Bongiovanni Laura⁵^ORCID,Thomas Rachel E.⁵,Bruin Alain¹⁵^ORCID,Sluis Bart¹^ORCID,Oosterveer Maaike H.¹^ORCID

Affiliation:

1. Department of Pediatrics University Medical Center GroningenUniversity of Groningen Groningen The Netherlands

2. Section of Metabolic Diseases Beatrix Children’s HospitalUniversity Medical Center Groningen Groningen The Netherlands

3. Department of Laboratory Medicine University Medical Center GroningenUniversity of Groningen Groningen The Netherlands

4. Central Animal Facility Groningen Small Animal Imaging Facility (Gronsai) University Medical Center GroningenUniversity of Groningen Groningen The Netherlands

5. Dutch Molecular Pathology Center Faculty of Veterinary Medicine Utrecht University CL Utrecht The Netherlands

Publisher

Wiley

Subject

Hepatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/hep.32022

Reference48 articles.

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2. Lessons from new mouse models of glycogen storage disease type 1a in relation to the time course and organ specificity of the disease

3. Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I)

4. Consensus guidelines for management of glycogen storage disease type 1b ‐ European study on glycogen storage disease type 1;Visser G;Eur J Pediatr,2002

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