Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects

A Boel; Joyce Burger; M Vanhomwegen; A Beyens; M Renard; Sander Barnhoorn; C Casteleyn; DP Reinhardt; B Descamps; C Vanhove; Ingrid Pluijm; P Coucke; A Willaert; J Essers; B Callewaert

doi:10.1093/hmg/ddaa071

Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects

A Boel, Joyce Burger, M Vanhomwegen, A Beyens, M Renard, Sander Barnhoorn, C Casteleyn, DP Reinhardt, B Descamps, C Vanhove, Ingrid Pluijm, P Coucke, A Willaert, J Essers, B Callewaert

Research output: Contribution to journal › Article › Academic › peer-review

7 Citations (Scopus)

Original language	English
Pages (from-to)	1476-1488
Number of pages	13
Journal	Human Molecular Genetics
Volume	29
Issue number	9
DOIs	https://doi.org/10.1093/hmg/ddaa071
Publication status	Published - 2020

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EMC MGC-01-12-03
EMC OR-01

Access to Document

10.1093/hmg/ddaa071

http://hdl.handle.net/1765/127932

Cite this

Boel, A., Burger, J., Vanhomwegen, M., Beyens, A., Renard, M., Barnhoorn, S., Casteleyn, C., Reinhardt, DP., Descamps, B., Vanhove, C., Pluijm, I., Coucke, P., Willaert, A., Essers, J., & Callewaert, B. (2020). Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects. Human Molecular Genetics, 29(9), 1476-1488. https://doi.org/10.1093/hmg/ddaa071

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title = "Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects",

author = "A Boel and Joyce Burger and M Vanhomwegen and A Beyens and M Renard and Sander Barnhoorn and C Casteleyn and DP Reinhardt and B Descamps and C Vanhove and Ingrid Pluijm and P Coucke and A Willaert and J Essers and B Callewaert",

year = "2020",

doi = "10.1093/hmg/ddaa071",

language = "English",

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Boel, A, Burger, J, Vanhomwegen, M, Beyens, A, Renard, M, Barnhoorn, S, Casteleyn, C, Reinhardt, DP, Descamps, B, Vanhove, C, Pluijm, I, Coucke, P, Willaert, A, Essers, J & Callewaert, B 2020, 'Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects', Human Molecular Genetics, vol. 29, no. 9, pp. 1476-1488. https://doi.org/10.1093/hmg/ddaa071

TY - JOUR

T1 - Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects

AU - Boel, A

AU - Burger, Joyce

AU - Vanhomwegen, M

AU - Beyens, A

AU - Renard, M

AU - Barnhoorn, Sander

AU - Casteleyn, C

AU - Reinhardt, DP

AU - Descamps, B

AU - Vanhove, C

AU - Pluijm, Ingrid

AU - Coucke, P

AU - Willaert, A

AU - Essers, J

AU - Callewaert, B

PY - 2020

Y1 - 2020

U2 - 10.1093/hmg/ddaa071

DO - 10.1093/hmg/ddaa071

M3 - Article

SN - 0964-6906

VL - 29

SP - 1476

EP - 1488

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 9

ER -