Novel mutations in SLC30A2 involved in the pathogenesis of transient neonatal zinc deficiency-Reference-Cited by-同舟云学术

Novel mutations in SLC30A2 involved in the pathogenesis of transient neonatal zinc deficiency

Published:2016-05-16 Issue:4 Volume:80 Page:586-594
ISSN:0031-3998
Container-title:Pediatric Research
language:en
Short-container-title:Pediatr Res

Author:

Itsumura Naoya,Kibihara Yoshie,Fukue Kazuhisa,Miyata Akiko,Fukushima Kenji,Tamagawa-Mineoka Risa,Katoh Norito,Nishito Yukina,Ishida Riko,Narita Hiroshi,Kodama Hiroko,Kambe Taiho^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://www.nature.com/articles/pr2016108.pdf

Reference40 articles.

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2. Fukada T, Kambe T. Molecular and genetic features of zinc transporters in physiology and pathogenesis. Metallomics 2011;3:662–74.

3. Hambidge KM, Krebs NF, Westcott JE, Miller LV. Changes in zinc absorption during development. J Pediatr 2006;149:5 Suppl:S64–8.

4. Krebs NF. Update on zinc deficiency and excess in clinical pediatric practice. Ann Nutr Metab 2013;62:Suppl 1:19–29.

5. Kelleher SL, Seo YA, Lopez V. Mammary gland zinc metabolism: regulation and dysregulation. Genes Nutr 2009;4:83–94.

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