Clinical features of 27 turkish propionic acidemia patients with 12 novel mutations-Reference-Cited by-同舟云学术

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Clinical features of 27 turkish propionic acidemia patients with 12 novel mutations

Published:2019 Issue:3 Volume:61 Page:330
ISSN:0041-4301
Container-title:The Turkish Journal of Pediatrics
language:
Short-container-title:TurkJPediatr

Author:

Kör Deniz,Şeker-Yılmaz Berna,Bulut Fatma Derya,Kılavuz Sebile,Öktem Murat,Ceylaner Serdar,Yıldızdaş Dinçer,Önenli-Mungan Neslihan

Publisher

The Turkish Journal of Pediatrics

Subject

Pediatrics, Perinatology, and Child Health

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Prevalence of propionic acidemia in China;Orphanet Journal of Rare Diseases;2023-09-09

2. Pathophysiological mechanisms of complications associated with propionic acidemia;Pharmacology & Therapeutics;2023-09

3. The debut and course of the neonatal form of propionic aciduria: a clinical case;L.O. Badalyan Neurological Journal;2023-06-30

4. Identification and characterization of the largest deletion in the PCCA gene causing severe acute early-onset form of propionic acidemia;Molecular Genetics and Genomics;2023-05-02

5. Clinical Characteristics and Genetic Analysis of a Case of Neonatal Early-Onset Propionate Acidemia and Literature Review;Advances in Clinical Medicine;2023

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