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Four-decade-old mummified umbilical tissue making retrospective molecular diagnosis of ornithine carbamoyltransferase deficiency

  • Published:2014-08-13 Issue:10 Volume:164 Page:2679-2681
  • ISSN:1552-4825
  • Container-title:American Journal of Medical Genetics Part A
  • language:en
  • Short-container-title:Am. J. Med. Genet.

Author:

Takenouchi Toshiki1,Tsukahara Yuki2,Horikawa Reiko3,Kosaki Kenjiro4,Kosaki Rika5

Affiliation:

1. Department of Pediatrics; Keio University School of Medicine; Tokyo Japan

2. Center for Maternal-Fetal; Neonatal and Reproductive Medicine; National Center for Child Health and Development; Tokyo Japan

3. Division of Endocrinology and Metabolism; National Center for Child Health and Development; Tokyo Japan

4. Center for Medical Genetics; Keio University School of Medicine; Tokyo Japan

5. Division of Medical Genetics; National Center for Child Health and Development; Tokyo Japan

Funder

Research on Applying Health Technology

Ministry of Health

Labor and Welfare

National Center for Child Health and Development

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 1 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. Ornithine transcarbamylase deficiency of a male newborn with fatal outcome;International Journal of Legal Medicine;2016-01-11
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