Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases-Reference-Cited by-同舟云学术

Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases

Published:2021-09 Issue:9 Volume:23 Page:1604-1615
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Rossignol Francis,Duarte Moreno Marvid S.,Benoist Jean-François,Boehm Manfred,Bourrat Emmanuelle,Cano Aline,Chabrol Brigitte,Cosson Claudine,Díaz José Luís Dapena,D’Harlingue Arthur,Dimmock David,Freeman Alexandra F.,García María Tallón,Garganta Cheryl,Goerge Tobias,Halbach Sara S.,de Laffolie Jan,Lam Christina T.,Martin Ludovic,Martins Esmeralda,Meinhardt Andrea,Melki Isabelle,Ombrello Amanda K.,Pérez Noémie,Quelhas Dulce,Scott Anna,Slavotinek Anne M.,Soares Ana Rita,Stein Sarah L.,Süßmuth Kira,Thies Jenny,Ferreira Carlos R.^ORCID,Schiff Manuel

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

https://www.nature.com/articles/s41436-021-01200-2.pdf

Reference157 articles.

1. Agence d’évaluation des technologies et des modes d’intervention en santé (AETMIS). La pertinence du dépistage néonatal urinaire des erreurs innées du métabolisme réalisé au Québec;Renaud,2009

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