Zobrazeno 1 - 2
of 2
pro vyhledávání: '"G D, Frechtel"'
Autor:
Ariel Pablo Lopez, F. M. Puchulu, M. S. Pérez, G. D. Frechtel, G. Krochik, I. Bergada, M. Rodríguez, V. Hirschler, S. A. Foscaldi, M. Traversa
Publikováno v:
Experimental and clinical endocrinologydiabetes : official journal, German Society of Endocrinology [and] German Diabetes Association. 117(8)
INTRODUCTION: Mutations in the glucokinase gene (GCK) produce a subtype of Maturity onset diabetes in the young (MODY), named MODY 2. To date over than 190 different mutations have been identified, distributed over the coding regions and the exon-int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dc22de506308a2f3da1f45bca0b5d5e
https://pubmed.ncbi.nlm.nih.gov/19358091
https://pubmed.ncbi.nlm.nih.gov/19358091
Autor:
H M, Targovnik, V, Varela, G D, Frechtel, G E, Cerrone, S B, Copelli, F V, Propato, F, Mendive
Publikováno v:
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas. 27(12)
1. Hereditary goiter and the various degrees of thyroid hypofunction are the result of structural changes in the thyroglobulin (Tg) or thyroperoxidase (TPO) proteins, the inability to couple iodotyrosines or defective iodination, impairing or substan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9c3d87ab464824a9cdd2b35205a8a47c
https://pubmed.ncbi.nlm.nih.gov/7549998
https://pubmed.ncbi.nlm.nih.gov/7549998