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Disease Models & Mechanisms
(May 2023)
Maternal heterozygosity of Slc6a19 causes metabolic perturbation and congenital NAD deficiency disorder in mice
Hartmut Cuny,
Kayleigh Bozon,
Rosemary B. Kirk,
Delicia Z. Sheng,
Stefan Bröer,
Sally L. Dunwoodie
Affiliations
Hartmut Cuny
Developmental and Stem Cell Biology Division, Victor Chang Cardiac Research Institute, Sydney, NSW 2010, Australia
Kayleigh Bozon
Developmental and Stem Cell Biology Division, Victor Chang Cardiac Research Institute, Sydney, NSW 2010, Australia
Rosemary B. Kirk
Developmental and Stem Cell Biology Division, Victor Chang Cardiac Research Institute, Sydney, NSW 2010, Australia
Delicia Z. Sheng
Developmental and Stem Cell Biology Division, Victor Chang Cardiac Research Institute, Sydney, NSW 2010, Australia
Stefan Bröer
Research School of Biology, Australian National University, Canberra, ACT 0200, Australia
Sally L. Dunwoodie
Developmental and Stem Cell Biology Division, Victor Chang Cardiac Research Institute, Sydney, NSW 2010, Australia
DOI
https://doi.org/10.1242/dmm.049647
Journal volume & issue
Vol. 16, no. 5
Abstract
Read online
No abstracts available.
Keywords
congenital malformation
miscarriage
nad
metabolism
embryonic development
tryptophan
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