Molecular Diagnosis of Hereditary Fructose Intolerance: Founder Mutation in a Community from India-Reference-Cited by-同舟云学术

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Molecular Diagnosis of Hereditary Fructose Intolerance: Founder Mutation in a Community from India

Published:2014 Issue: Volume: Page:85-93
ISSN:2192-8304
Container-title:JIMD Reports
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Author:

Bijarnia-Mahay Sunita,Movva Sireesha,Gupta Neerja,Sharma Deepak,Puri Ratna D.,Kotecha Udhaya,Saxena Renu,Kabra Madhulika,Mohan Neelam,Verma Ishwar C

Publisher

Springer Berlin Heidelberg

Link

http://link.springer.com/content/pdf/10.1007/8904_2014_374

Reference19 articles.

1. Ananth N, Praveenkumar GS, Rao KA, Vasanthi, Kakkilaya S (2003) Two cases of hereditary fructose intolerance. Indian J Clin Biochem 18(2):87–92

2. Ankala A, Kohn JN, Dastur R, Gaitonde P, Khadilkar SV, Hegde MR (2013) Ancestral founder mutations in calpain-3 in the Indian Agarwal community: historical, clinical, and molecular perspective. Muscle Nerve 47(6):931–937

3. Bahl S, Virdi K, Mittal U, Sachdeva MP, Kalla AK, Holmes SE, O’Hearn E, Margolis RL, Jain S, Srivastava AK, Mukerji M (2005) Evidence of a common founder for SCA12 in the Indian population. Ann Hum Genet 69:528–534

4. Bharadia L, Shivpuri D (2012) Non responsive celiac disease due to coexisting hereditary fructose intolerance. Indian J Gastroenterol 31(2):83–84

5. Blanco E, Parra G, Guigó R (2007) Using gene id to identify genes. Curr Protoc Bioinformatics. doi: 10.1002/0471250953.bi0403s18

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