Late‐onset of ornithine transcarbamylase deficiency: A rare medical examiner case-Reference-Cited by-同舟云学术

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Late‐onset of ornithine transcarbamylase deficiency: A rare medical examiner case

Published:2021-11-02 Issue: Volume: Page:
ISSN:0022-1198
Container-title:Journal of Forensic Sciences
language:en
Short-container-title:J Forensic Sci

Author:

Gitto Lorenzo¹^ORCID,Fuller Cristine E.¹,Calleo Vincent J.²,Tawil Michel¹,Thach Rasmey³,Revercomb Carolyn⁴

Affiliation:

1. Department of Pathology SUNY Upstate Medical University Syracuse New York USA

2. Upstate New York Poison Center SUNY Upstate Medical University Syracuse New York USA

3. Department of Medicine William Beaumont Army Medical Center Fort Bliss Texas USA

4. Onondaga County Medical Examiner's Office Syracuse New York USA

Publisher

Wiley

Subject

Genetics,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1556-4029.14934

Reference25 articles.

1. Genotype spectrum of ornithine transcarbamylase deficiency: Correlation with the clinical and biochemical phenotype

2. Neuropsychological attributes of urea cycle disorders: A systematic review of the literature

3. High-frequency detection of deletions and variable rearrangements at the ornithine transcarbamylase (OTC) locus by oligonucleotide array CGH

4. National organization for rare disorders (NORD).Ornithine transcarbamylase deficiency.2015.http://rarediseases.org/rare‐diseases/ornithine‐transcarbamylase‐deficiency. Accessed 24 Aug 2021.

5. Long-Term Treatment of Girls with Ornithine Transcarbamylase Deficiency

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