Fanconi-Bickel Syndrome: Another Novel Mutation in SLC2A2
Author:
Funder
Indian Council of Medical Research
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s12098-016-2236-6.pdf
Reference5 articles.
1. Santer R, Groth S, Kinner M, et al. The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome. Hum Genet. 2002;110:21–9.
2. Al-Haggar M, Sakamoto O, Shaltout A, Al-Hawari A, Wahba Y, Abdel-Hadi D. Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi-Bickel syndrome: revisited gene atlas for renumbering. Clin Exp Nephrol. 2012;16:604–10.
3. Mohandas Nair K, Sakamoto O, Jagadeesh S, Nampoothiri S. Fanconi-Bickel syndrome. Indian J Pediatr. 2012;79:112–4.
4. Ekbote AV, Mandal K, Agarwal I, Sinha R, Danda S. Fanconi-Bickel syndrome: mutation in an Indian patient. Indian J Pediatr. 2012;79:810–2.
5. Kehar M, Bijarnia S, Ellard S, et al. Fanconi-Bickel syndrome - mutation in SLC2A2 gene. Indian J Pediatr. 2014;81:1237–9.
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