Genetische Defekte des Monosaccharidstoffwechsels
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-54671-6_73-2
Reference18 articles.
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2. Berry GT, Walter JH, Fridovich-Keil JL (2016) Disorders of galactose metabolism. In: Saudubray JM, Baumgartner M, Walter J (Hrsg) Inborn metabolic diseases: diagnosis and treatment, 6. Aufl. Springer, Heidelberg, S 139–147
3. Carlock G, Fischer ST, Lynch ME et al (2019) Developmental outcomes in Duarte galactosemia. Pediatrics 143:e20182516
4. Coady MJ, El Tarazi A, Santer R et al (2017) MAP17 is a necessary activator of renal Na+/glucose cotransporter SGLT2. J Am Soc Nephrol 28:85–93
5. De Leon DD, Stanley CA (2017) Congenital hypoglycemia disorders: new aspects of etiology, diagnosis, treatment and outcomes: highlights of the proceedings of the congenital hypoglycemia disorders symposium, Philadelphia April 2016. Pediatr Diabetes 18:3–9
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