Linkage between I172N mutation, a marker of 21-hydroxylase deficiency, and a single nucleotide polymorphism in Int6 of CYP21B gene: A genetic study of Sardinian family
| Autor: | Concolino, Paola, Satta, Maria Antonia, Santonocito, Concetta, Carrozza, Cinzia, Rocchetti, Sandro, Ameglio, Franco, Giardina, Emiliano, Zuppi, Cecilia, Capoluongo, Ettore |
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| Zdroj: | In Clinica Chimica Acta 2006 364(1):298-302 |
| Databáze: | ScienceDirect |
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