Point mutations in Italian patients with classic, non-classic, and cryptic forms of steroid 21-hydroxylase deficiency

Paola Carrera1,2, Laura Bordone1,2, Tiziana Azzani2,1, Valeria Brunelli3, Maria Paola Garancini4, G Chiumello3, Maurizio Ferrari1,2
1Fax: +39 2 26432640, , IT
2Laboratorio di Biologia Molecolare Clinica, I.R.C.C.S. H S. Raffaele, via Olgettina, 60, I-20132, Milan, Italy Tel.: +39 2 26432617
3Clinica Pediatrica III, Università di Milano, Milan, Italy, , IT
4I.R.C.C.S. H S. Raffaele, Epidemiology Unit, Milan, Italy, IT

Tóm tắt

Từ khóa


Tài liệu tham khảo