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Androgen insensitivity syndrome (AIS) results from failure of masculinization of target organs by androgen secretions during embryo development.
Specifications
Breeds | |
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Gene | |
Organ | |
specimen | Hair, Blood EDTA, Blood Heparin, Semen, Tissue |
Mode of Inheritance | |
Chromosome | |
Also known as | |
Year Published |
General information
Androgen insensitivity syndrome (AIS) results from failure of masculinization of target organs by androgen secretions during embryo development. The mutation is caused by a 25-bp deletion on the DNA-binding domain of the androgen receptor gene in the family.