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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

Document Type

Journal

Author

Concolino, P; Satta, MA; Santonocito, C; Carrozza, C; Rocchetti, S; Ameglio, F; Giardina, E; Zuppi, C; Capoluongo, E

Source

CLINICA CHIMICA ACTA; FEB 2006, 364 1-2, p298-p302, 5p.

Subject

Language

English

ISSN

00098981

Online Access

Full Text (ScienceDirect) Web of Science JCR 저널정보 Scopus Find it@PNU

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