Congenital Glucose-Galactose Malabsorption: A Case With a Novel SLC5A1 Mutation in a Saudi Infant-Reference-Cited by-同舟云学术

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Congenital Glucose-Galactose Malabsorption: A Case With a Novel SLC5A1 Mutation in a Saudi Infant

Published:2021-10-02 Issue: Volume: Page:
ISSN:2168-8184
Container-title:Cureus
language:en
Short-container-title:

Author:

Alamoudi Loujen O,Alfaraidi Albaraa T,Althagafi Samiyah S,Al-Thaqafy Majid S,Hasosah Mohammed

Publisher

Cureus, Inc.

Subject

Aerospace Engineering

Reference15 articles.

1. Genes and Disease;National Center for Biotechnology Information (US),1998

2. I. Glucose galactose malabsorption;Wright EM;Am J Physiol,1998

3. Literature review on congenital glucose-galactose malabsorption from 2001 to 2019;Wang W;J Paediatr Child Health,2020

4. Molecular basis for glucose-galactose malabsorption;Wright EM;Cell Biochem Biophys,2002

5. The Na(+)/glucose cotransporters: from genes to therapy;Sabino-Silva R;Braz J Med Biol Res,2010

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Gastrointestinal lactose intolerance;Galenika Medical Journal;2024

2. Genetic Variants in Carbohydrate Digestive Enzyme and Transport Genes Associated with Risk of Irritable Bowel Syndrome;2023-09-22

3. SLC5A1 Variants in Turkish Patients with Congenital Glucose-Galactose Malabsorption;Genes;2023-06-27

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