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Homozygous Rare PARN Missense Mutation in Familial Pulmonary Fibrosis.
David Zhang
Zhengyang Zhou
Muhanned Abu-Hijleh
Kiran Batra
Chao Xing
Christine Kim Garcia
Published in:
American journal of respiratory and critical care medicine (2020)
Keyphrases
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pulmonary fibrosis
intellectual disability
early onset
autism spectrum disorder