Mutational assessment in nkx2-5 and actc1 genesin patients with congenital cardiac septal defect (ccsd)from ethnic kashmiri population

HIGHLIGHTS

• who: Nadeem Ul Nazeer and colleagues from the Department of CVTS, Sheri-Kashmir Institute of Medical Sciences, Srinagar, India have published the paper: Mutational Assessment in NKX2-5 and ACTC1 Genesin Patients with Congenital Cardiac Septal Defect (CCSD)from Ethnic Kashmiri Population, in the Journal: (JOURNAL)
• what: This study evaluates the role of key hotspot mutations in NKX2-5 and ACTC1 genes of congenital cardiac septal defect (CCSD) in ethnic Kashmiri population. This study was designed and conducted in the Department of Cardiovascular Thoracic Surgery (CVTS) and Advanced Centre for Human Genetics, Sheri Kashmir Institute . . .
  

   

  

  If you want to have access to all the content you need to log in!

  Thanks :)

  Username or E-mail:

  If you don't have an account, you can create one here.