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About this Medicine article
Whole‐exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations by Sanga, Shamita; Ghosh, Arnab; Kumar, Krishna; Polavarapu, Kiran; Kumar, Veeramani P.; Vengalil, Seena; Nashi, Saraswati; Bardhan, Mainak; Arunachal, Gautham; Raju, Sanita; Gayathri, Narayanappa; Biswas, Nidhan K.; Chakrabarti, Saikat; Nalini, Atchayaram; Roy, Sudipto; Acharya, Moulinath is a Medicine article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Medicine.
- Author
- Sanga, Shamita; Ghosh, Arnab; Kumar, Krishna; Polavarapu, Kiran; Kumar, Veeramani P.; Vengalil, Seena; Nashi, Saraswati; Bardhan, Mainak; Arunachal, Gautham; Raju, Sanita; Gayathri, Narayanappa; Biswas, Nidhan K.; Chakrabarti, Saikat; Nalini, Atchayaram; Roy, Sudipto; Acharya, Moulinath
- Publisher
- John Wiley and Sons; Wiley (Blackwell Publishing); Blackwell Publishing Inc.; Wiley (ISSN 1351-5101)
- Published
- 2020
- Field
- Medicine (Health Sciences)