Literature DB >> 14514278

Dystrophin gene deletions in South Indian Duchenne muscular dystrophy patients.

G N Mallikarjuna Rao1, T Hussain, N Geetha Devi, Suman Jain, G R Chandak, M P J S Ananda Raj.   

Abstract

66 unrelated patients from Southern India with Duchenne Muscular Dystrophy (DMD) were studied for intragenic deletion in 18 exons and Pm region of the DMD gene using multiplex PCR. Of these 41 (62.1%) showed intragenic deletions. 78% of the deletions were located at the distal hotspot region (44-55 exons) and 22% of the deletions were located at the proximal region (exon 2-19). Exon 50 is most frequently deleted. Deletions in isolated cases were significantly more compared to familial cases. The lower incidence reported from South India compared to North India, is suggestive of variations in the Southern and Northern population.

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Year:  2003        PMID: 14514278

Source DB:  PubMed          Journal:  Indian J Med Sci        ISSN: 0019-5359


  4 in total

1.  MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India.

Authors:  Sekar Deepha; Seena Vengalil; Veeramani Preethish-Kumar; Kiran Polavarapu; Atchayaram Nalini; Narayanappa Gayathri; Meera Purushottam
Journal:  BMC Med Genet       Date:  2017-06-13       Impact factor: 2.103

2.  Study of Dystrophinopathy in Eastern Uttar Pradesh Population of India.

Authors:  Preeti Kumari; Deepika Joshi; Satya N Shamal; Royana Singh
Journal:  J Pediatr Neurosci       Date:  2018 Apr-Jun

3.  Duchenne Muscular Dystrophy: Genetic and Clinical Profile in the Population of Rajasthan, India.

Authors:  Manisha Goyal; Ashok Gupta; Kamlesh Agarwal; Seema Kapoor; Somesh Kumar
Journal:  Ann Indian Acad Neurol       Date:  2021-08-20       Impact factor: 1.383

Review 4.  Muscular dystrophies.

Authors:  Monisha Mukherjee; Balraj Mittal
Journal:  Indian J Pediatr       Date:  2004-02       Impact factor: 5.319

  4 in total

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