Case series of Arginase 1 deficiency: Expanding the spectrum in hyperargininemia-Reference-Cited by-同舟云学术

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Case series of Arginase 1 deficiency: Expanding the spectrum in hyperargininemia

Published:2021-08-03 Issue: Volume: Page:
ISSN:1328-8067
Container-title:Pediatrics International
language:en
Short-container-title:Pediatrics International

Author:

Dorum Sevil¹^ORCID,Havalı Cengiz²

Affiliation:

1. Medical Doctor Department of Pediatrics Division of Metabolism Bursa Yuksek Ihtisas Training and Research Hospital Bursa Turkey

2. Medical Doctor Department of Pediatrics Division of Pediatric Neurology Bursa Yuksek Ihtisas Training and Research Hospital Bursa Turkey

Publisher

Wiley

Subject

Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ped.14945

Cited by 3 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. Argininemia: Pathophysiology and Novel Methods for Evaluation of the Disease;Applied Sciences;2024-02-18

2. ACMG/AMP variant classification framework in arginase 1 deficiency: Implications for birth prevalence estimates and diagnostics;Genetics in Medicine Open;2024

3. Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia.;Molecular Case Studies;2022-09-30

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