Relevance of solute carrier family 5 transporter defects to inherited and acquired human disease
Author:
Funder
SCORE research exchange program
Publisher
Springer Science and Business Media LLC
Subject
Genetics,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s13353-019-00502-1.pdf
Reference73 articles.
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2. Altorjay A, Dohán O, Szilágyi A et al (2007) Expression of the Na+/I− symporter (NIS) is markedly decreased or absent in gastric cancer and intestinal metaplastic mucosa of Barrett esophagus. BMC Cancer 7(5). https://doi.org/10.1186/1471-2407-7-5
3. Anderson S, Koniaris S, Baozhong Xin B et al (2017) Congenital glucose–galactose malabsorption: a case report. J Pediatr Health Care 31(4). https://doi.org/10.1016/j.pedhc.2017.01.005
4. Askanas V, Engel WK, Nogalska A (2015) Sporadic inclusion-body myositis: a degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy. Biochim Biophys Acta 1852:633–643. https://doi.org/10.1016/j.bbadis.2014.09.005
5. Assiri A, Saeed A, Alnimri A et al (2013) Five Arab children with glucose-galactose malabsorption. P Paediatr Int Child Health 33:108–110. https://doi.org/10.1179/2046905513Y.0000000055
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