P492: Identification of molecular modifiers of disease in a group of systematically phenotyped patients with cystic fibrosis

• Gurpreet Kaur,
• Donna Brown,
• Brandon Wilk,
• Manavalan Gajapathy,
• Tarun Karthik Mamidi,
• Shaurita Hutchins,
• Camille Birch,
• Felipe Massicano,
• Jinmyung Choi,
• Sangita Murali,
• Huichuan Lai,
• Philip Farrell,
• Elizabeth Worthey

Affiliations

Gurpreet Kaur

Marnix E. Heersink School of Medicine, University of Alabama, Birmingham, AL

Donna Brown

Marnix E. Heersink School of Medicine, University of Alabama, Birmingham, AL

Brandon Wilk

Marnix E. Heersink School of Medicine, University of Alabama, Birmingham, AL

Manavalan Gajapathy

Marnix E. Heersink School of Medicine, University of Alabama, Birmingham, AL

Tarun Karthik Mamidi

Marnix E. Heersink School of Medicine, University of Alabama, Birmingham, AL

Shaurita Hutchins

Marnix E. Heersink School of Medicine, University of Alabama, Birmingham, AL

Camille Birch

Marnix E. Heersink School of Medicine, University of Alabama, Birmingham, AL

Felipe Massicano

Marnix E. Heersink School of Medicine, University of Alabama, Birmingham, AL

Jinmyung Choi

Marnix E. Heersink School of Medicine, University of Alabama, Birmingham, AL

Sangita Murali

University of Wisconsin, Madison, WI

Huichuan Lai

University of Wisconsin, Madison, WI

Philip Farrell

University of Wisconsin, Madison, WI

Elizabeth Worthey

Marnix E. Heersink School of Medicine, University of Alabama, Birmingham, AL