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Mutations in the V‐ATPase assembly factor VMA21 cause a congenital disorder of glycosylation with autophagic liver disease

Lookup NU author(s): Professor Joris VeltmanORCiD

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This is the authors' accepted manuscript of an article that has been published in its final definitive form by John Wiley & Sons, Inc. , 2020.

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Author(s): Serio MC, Graham LA, Ashikov A, Larsen LA, Raymond K, Timal S, Meur G, Ryan M, Czarnowska E, Jansen JC, He M, Ficicioglu C, Pichurin P, Hasadsri L, RiosOcampo WA, Gilissen C, Rodenburg R, Jonker JW, Holleboom AG, Morava E, Veltman JA, Socha P, Stevens TH, Simons M, Lefeber DJ

Publication type: Article

Publication status: Published

Journal: Hepatology

Year: 2020

Volume: 72

Issue: 6

Pages: 1968-1986

Print publication date: 01/12/2020

Online publication date: 07/03/2020

Acceptance date: 17/02/2020

Date deposited: 24/06/2020

ISSN (print): 0270-9139

ISSN (electronic): 1527-3350

Publisher: John Wiley & Sons, Inc.

URL: https://doi.org/10.1002/hep.31218

DOI: 10.1002/hep.31218

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