O.J.C. Hellwinkel, K. Bull, P.M. Holterhus, N. Homberg, D. Struve, O. Hiort. Complete androgen insensitivity caused by a splice donor site mutation in intron 2 of the human androgen receptor gene resulting in an exon 2-lacking transcript with premature stop-codon and reduced expression. Journal of Steroid Biochemistry and Molecular Biology Vol 68 (1999) 1–9

• Book ID: 117669215
• Publisher: Elsevier Science
• Year: 1999
• Tongue: English
• Weight: 70 KB
• Volume: 71
• Category: Article
• ISSN: 0960-0760
• DOI: 10.1016/s0960-0760(99)00098-9