Novel de novo pathogenic variant in the ODC1 gene in a girl with developmental delay, alopecia, and dysmorphic features-Reference-Cited by-同舟云学术

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Novel de novo pathogenic variant in the ODC1 gene in a girl with developmental delay, alopecia, and dysmorphic features

Published:2018-09-21 Issue:12 Volume:176 Page:2548-2553
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Bupp Caleb P.¹²,Schultz Chad R.²,Uhl Katie L.²,Rajasekaran Surender²³,Bachmann André S.²^ORCID

Affiliation:

1. Medical Genetics, Spectrum Health and Helen DeVos Children's Hospital; Grand Rapids Michigan

2. Department of Pediatrics and Human Development; College of Human Medicine, Michigan State University; Grand Rapids Michigan

3. Pediatric Critical Care Medicine; Helen DeVos Children's Hospital; Grand Rapids Michigan

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.40523/fullpdf

Reference23 articles.

1. Crystal structure of human ornithine decarboxylase at 2.1 a resolution: Structural insights to antizyme binding;Almrud;Journal of Molecular Biology,2000

2. Targeting polyamine metabolism and function in cancer and other hyperproliferative diseases;Casero;Nature Reviews Drug Discovery,2007

3. Pattern of blood polyamines in healthy subjects from infancy to the adult age;Casti;Journal of Endocrinological Investigation,1982

4. Polyamines and cancer: Old molecules, new understanding;Gerner;Nature Reviews Cancer,2004

5. Prevention of rapid intracellular degradation of ODC by a carboxyl-terminal truncation;Ghoda;Science,1989

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