← Evidence map

ArticleERJ open research2019

Prolidase deficiency diagnosed by whole exome sequencing in a child with pulmonary capillaritis.

Jonathan H Rayment et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

7 papers cite it

2019
2020
2021
2022
2023
2024
2025
this paperpooled itcites it
Full record →Abstract, authors, funding and every citing paper · PMID 31041317