A novel surfactant protein C gene mutation associated with progressive respiratory failure in infancy.
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Gene Editing and Genetic Lung Disease. Basic Research Meets Therapeutic Application.Transthyretin and BRICHOS: The Paradox of Amyloidogenic Proteins with Anti-Amyloidogenic Activity for Aβ in the Central Nervous System.Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotype.Pediatric Case Report on an Interstitial Lung Disease with a Novel Mutation of SFTPC Successfully Treated with Lung Transplantation.
P2860
A novel surfactant protein C gene mutation associated with progressive respiratory failure in infancy.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
A novel surfactant protein C g ...... espiratory failure in infancy.
@en
type
label
A novel surfactant protein C g ...... espiratory failure in infancy.
@en
prefLabel
A novel surfactant protein C g ...... espiratory failure in infancy.
@en
P2093
P2860
P356
P1476
A novel surfactant protein C g ...... espiratory failure in infancy.
@en
P2093
Geoffrey Kurland
Lawrence M Nogee
Melissa Kaori Silva Litao
Saurabh Chiwane
P2860
P356
10.1002/PPUL.23493
P577
2016-06-30T00:00:00Z