Transient Neonatal Zinc Deficiency Caused by a Heterozygous G87R Mutation in the Zinc Transporter ZnT-2 (SLC30A2) Gene in the Mother Highlighting the Importance of Zn2+ for Normal Growth and Development.
Autor: | Miletta, Maria Consolata1, Bieri, Andreas1, Kernland, Kristin2, Schöni, Martin H.1, Petkovic, Vibor1, Flück, Christa E.1, Eblé, Andrée1, Mullis, Primus E.1 primus.mullis@insel.ch |
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Zdroj: | International Journal of Endocrinology. 2013, p1-8. 8p. |
Databáze: | Academic Search Ultimate |
Externí odkaz: |