Complete androgen insensitivity caused by a splice donor site mutation in intron 2 of the human androgen receptor gene resulting in an exon 2-lackingtranscript with premature stop-codon and reduced expression (vol 68, pg 1,1999)
Ojc. Hellwinkel et al., Complete androgen insensitivity caused by a splice donor site mutation in intron 2 of the human androgen receptor gene resulting in an exon 2-lackingtranscript with premature stop-codon and reduced expression (vol 68, pg 1,1999), J STEROID B, 71(1-2), 1999, pp. 91-91
Citations number
1
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY