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

✍ Scribed by Olaf José-Carlos Hellwinkel; Kerstin Bull; Paul-Martin Holterhus; Nicole Homburg; Dagmar Struve; Olaf Hiort

• Book ID: 117669126
• Publisher: Elsevier Science
• Year: 1999
• Tongue: English
• Weight: 402 KB
• Volume: 68
• Category: Article
• ISSN: 0960-0760
• DOI: 10.1016/s0960-0760(98)00157-5