论文信息 - Targeted Next Generation Sequencing Identifies a Novel Deletion in LAMA2 Gene in a Merosin Deficient Congenital Muscular Dystrophy Patient - 字舞流文

Targeted Next Generation Sequencing Identifies a Novel Deletion in LAMA2 Gene in a Merosin Deficient Congenital Muscular Dystrophy Patient

A. Dalal | S. Aggarwal | A. D. Bhowmik | C. Sundaram | D. Matta

[1] M. Hegde,et al. Assessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophy. , 2012, The Journal of molecular diagnostics : JMD.

[2] S. Pascual-Pascual,et al. LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients , 2008, Clinical genetics.