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Event

Whole Exome Sequencing to Identify a Novel Mutation in SFTPA2 Associated with Familial Idiopathic Pulmonary Fibrosis [Board No. 924]

Location: Board no. 924
Session Type: RAPiD: Rapid Abstract Poster Discussion Session
Sunday
May
20
9:15 AM
11:15 AM

Speaker(s)/Author(s)

Hong Luo

MD, PhD
The second Xiangya Hospital of Central South University

Lyu Liu

DOCTOR
The Second Xiangya Hospital of Central South University

View Abstract

Whole Exome Sequencing to Identify a Novel Mutation in SFTPA2 Associated with Familial Idiopathic Pulmonary Fibrosis

Parent Sessions

  • A21 - CLINICAL AND MECHANISTIC STUDIES OF LUNG FIBROSIS...
    05-20-2018 9:15 AM - 11:15 AM
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