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

International Journal of Endocrinology

Volumn 2013, Issue , 2013, Pages

  Miletta, Maria Consolata ^a   Bieri, Andreas ^a   Kernland, Kristin ^b   Schöni, Martin H ^a   Petkovic, Vibor ^a   Flück, Christa E ^a   Eblé, Andrée ^a   Mullis, Primus E ^a  

^a UNIVERSITY CHILDREN S HOSPITAL   (Switzerland)

^b UNIVERSITY OF BERN   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; GROWTH HORMONE; ZINC TRANSPORTER;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD DEVELOPMENT; CHILD GROWTH; CYTOPLASM; DIETARY INTAKE; DNA ISOLATION; EXTRACELLULAR SPACE; GENE; GENE MUTATION; HETEROZYGOSITY; HOMEOSTASIS; HUMAN; INFANT NUTRITION; NEWBORN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SLC30A2 GENE; TRANSIENT NEONATAL ZINC DEFICIENCY; ZINC DEFICIENCY;

EID: 84886560544     PISSN: 16878337     EISSN: 16878345     Source Type: Journal    
DOI: 10.1155/2013/259189     Document Type: Article

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