Metabolic autopsy with next generation sequencing in sudden unexpected death in infancy: Postmortem diagnosis of fatty acid oxidation disorders-Reference-Cited by-同舟云学术

Metabolic autopsy with next generation sequencing in sudden unexpected death in infancy: Postmortem diagnosis of fatty acid oxidation disorders

Published:2015-12 Issue: Volume:5 Page:26-32
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Yamamoto Takuma,Mishima Hiroyuki,Mizukami Hajime,Fukahori Yuki,Umehara Takahiro,Murase Takehiko,Kobayashi Masamune,Mori Shinjiro,Nagai Tomonori,Fukunaga Tatsushige,Yamaguchi Seiji,Yoshiura Koh-ichiro,Ikematsu Kazuya

Funder

Ministry of Health, Labour and Welfare of Japan

Ministry of Education, Culture, Sports, Science and Technology of Japan

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference35 articles.

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4. Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life;Boles;J. Pediatr.,1998

5. Electrospray tandem mass spectrometry for analysis of acylcarnitines in dried postmortem blood specimens collected at autopsy from infants with unexplained cause of death;Chace;Clin. Chem.,2001

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