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Characterization of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene mutations in Indian patients with cystic fibrosis using Next Generation Sequencing (NGS) based approach & development of a cost effective strategy for mutation screening

Funding Organization
Funding Organization

Quick Information
Area of Research
Medical Sciences
Focus Area
Ad-hoc, ADHOC
Start Year
2019
End Year
2022
Sanction Amount
₹ 37.24 L
Status
Completed
Output
No. of Research Paper
00
Technologies (If Any)
00
No. of PhD Produced
N/A
Startup (If Any)
00
No. of Patents
Filed :00
Grant :00
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