Author:
Das Bhowmik Aneek,Rangaswamaiah Savithri,Srinivas G.,Dalal Ashwin B.
Funder
Centre for DNA Fingerprinting and Diagnostics
Subject
Genetics(clinical),Genetics,General Medicine
Reference52 articles.
1. Congenital myotonic dystrophy with asymptomatic mother;Anand;Indian Pediatr,2011
2. Molecular diagnosis of myotonic dystrophy and Huntington's disease from Calcutta, India;Basu;Neurol India,1998
3. Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India;Basu;Hum Genet,2000
4. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member;Brook;Cell,1992
5. Detection of large pathogenic expansions in FRDA1, SCA10, and SCA12 genes using a simple fluorescent repeat-primed PCR assay;Cagnoli;J Mol Diagn,2004
Cited by
6 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