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Autor:
Liliana B, Dain, Noemí D, Buzzalino, Adriana, Oneto, Susana, Belli, Mirta, Stivel, Titania, Pasqualini, Carolina, Minutolo, Eduardo H, Charreau, Liliana G, Alba
Publikováno v:
Clinical endocrinology. 56(2)
To characterize the molecular basis of the 21-hydroxylase deficiency in a group of Argentine patients presenting the classical and nonclassical forms of the disease.To analyse the frequency of point mutations in the CYP21 gene by DNA amplification an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::be2817fb50e6686c03ed602b3204d256
https://pubmed.ncbi.nlm.nih.gov/12580943
https://pubmed.ncbi.nlm.nih.gov/12580943
