𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Response to local dihydrotestosterone treatment in a patient with partial androgen-insensitivity syndrome due to a novel mutation in the androgen receptor gene

✍ Scribed by Foresta, Carlo ;Bettella, Andrea ;Ferlin, Alberto ;Garolla, Andrea ;Moro, Enrico ;Baldinotti, Fulvia ;Simi, Paolo ;Dallapiccola, Bruno


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
50 KB
Volume
107
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


A novel point mutation (R840S) in the an
✍ Karla F.S. Melo; Ana Claudia Latronico; Elaine M.F. Costa; Ana Elisa C. Billerbe πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 14 KB πŸ‘ 1 views

Mutations of the androgen receptor gene causing androgen insensitivity syndrome in 46, XY individuals, result in phenotypes ranging from complete female to ambiguous genitalia to males with minor degrees of undervirilization. We studied two Brazilian brothers with partial androgen insensitivity synd

Two novel mutant alleles of the gene enc
✍ Marek Bodzioch; Katarzyna Lapicka; Charalampos Aslanidis; Marek Kacinski; Gerd S πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 34 KB πŸ‘ 1 views

Congenital insensitivity to pain with anhidrosis (CIPA), also called hereditary sensory and autonomic neuropathy type IV (HSAN IV), is caused by mutations of the NTRK1 gene coding for the neurotrophic tyrosine kinase receptor type 1. We report the results of the NTRK1 sequence analysis in a CIPA fam