SLC5A1 Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption-Reference-Cited by-同舟云学术

SLC5A1 Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption

Published:2018-02 Issue:2 Volume:66 Page:250-252
ISSN:0277-2116
Container-title:Journal of Pediatric Gastroenterology & Nutrition
language:en
Short-container-title:

Author:

Al-Suyufi Yasir,ALSaleem Khalid,Al-Mehaidib Ali,Banemai Mohammed,Aldekhail Wajeeh M.,Al-Muhandes Abdulhakim,Mohammed Manal,Allam Rabab,Jambi Amani,Ramzan Khushnooda,Imtiaz Faiqa

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Pediatrics, Perinatology and Child Health

Reference21 articles.

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2. L’intolerance au lactose et le syndrome coeliaque;Laplane;Arch Franc Pediatr,1962

3. Congenital selective malabsorption of glucose and galactose;Evans;J Pediatr Gastroenterol Nutr,1985

4. Multiple sequence variations in SLC5A1 gene are associated with glucose-galactose malabsorption in a large cohort of Old Order Amish;Xin;Clin Genet,2011

5. Glucose galactose malabsorption;Wright;Am J Physiol,1998

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