Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity

Antzeko izenburuak

• Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
  nork: Lubahn, D B, et al.
  Argitaratua: (1989)
• An exonic point mutation of the androgen receptor gene in a family with complete androgen insensitivity
  nork: Sai, Tetsujun, et al.
  Argitaratua: (1990)
• Complete androgen insensitivity syndrome caused by a deep intronic pseudoexon-activating mutation in the androgen receptor gene
  nork: Känsäkoski, Johanna, et al.
  Argitaratua: (2016)
• Mutational analysis of the androgen receptor gene in two Chinese families with complete androgen insensitivity syndrome
  nork: WANG, SONG, et al.
  Argitaratua: (2016)
• Molecular analysis of the androgen-receptor gene in a family with receptor-positive partial androgen insensitivity: an unusual type of intronic mutation.
  nork: Brüggenwirth, H T, et al.
  Argitaratua: (1997)