Carrier detection in a partially dominant X-linked disease: ornithine transcarbamylase deficiency-Reference-Cited by-同舟云学术

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Carrier detection in a partially dominant X-linked disease: ornithine transcarbamylase deficiency

Published:1990-01 Issue:2 Volume:84 Page:
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Pelet Anna,Rotig Agn�s,Bona�ti-Pelli� Catherine,Rabier Daniel,Cormier Val�rie,Toumas Elias,Hentzen Dani�le,Saudubray Jean-Marie,Munnich Arnold

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00208934.pdf

Cited by 14 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. AAV gene therapy corrects OTC deficiency and prevents liver fibrosis in aged OTC-knock out heterozygous mice;Molecular Genetics and Metabolism;2017-04

2. Infusionstherapie und Ernährung bei angeborenen Stoffwechselstörungen;Ernährungsmedizin Pädiatrie;2012-12-19

3. Disorders of the Metabolism of Amino Acids and Related Compounds;Genetic Disorders and the Fetus;2010-09-24

4. Contiguous Xp11.4 Gene Deletion Leading to Ornithine Transcarbamylase Deficiency Detected by High-density Single-nucleotide Array;Clinical Pediatric Endocrinology;2010

5. Lethal ornithine transcarbamylase deficiency in a female neonate: a new case;Acta Paediatrica;2007-01-02

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