Partial androgen insensitivity syndrome caused by a deep intronic mutation creating an alternative splice acceptor site of the AR gene
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2045-2322
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Partial androgen insensitivity syndrome caused by a deep intronic mutation creating an alternative splice acceptor site of the AR gene ; volume:8 ; number:1 ; day:2 ; month:2 ; year:2018 ; pages:1-8 ; date:12.2018
Scientific reports ; 8, Heft 1 (2.2.2018), 1-8, 12.2018
- Urheber
-
Ono, Hiroyuki
- Beteiligte Personen und Organisationen
-
Saitsu, Hirotomo
Horikawa, Reiko
Nakashima, Shinichi
Ohkubo, Yumiko
Yanagi, Kumiko
Nakabayashi, Kazuhiko
Fukami, Maki
Fujisawa, Yasuko
Ogata, Tsutomu
SpringerLink (Online service)
- DOI
-
10.1038/s41598-018-20691-9
- URN
-
urn:nbn:de:101:1-2018090611072834422918
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:27 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Ono, Hiroyuki
- Saitsu, Hirotomo
- Horikawa, Reiko
- Nakashima, Shinichi
- Ohkubo, Yumiko
- Yanagi, Kumiko
- Nakabayashi, Kazuhiko
- Fukami, Maki
- Fujisawa, Yasuko
- Ogata, Tsutomu
- SpringerLink (Online service)
Ähnliche Objekte (12)
Embryonal carcinoma in androgen insensitivity syndrome
Androgen responsive intronic non-coding RNAs
Bilateral Breast Phyllodes Tumor in Androgen Insensitivity Syndrome
LINE1-mediated epigenetic repression of androgen receptor transcription causes androgen insensitivity syndrome
Two cases of androgen insensitivity due to somatic mosaicism
Complete Androgen Insensitivity Syndrome: Role of Imaging for Diagnosis
Genome-wide screening of biomarkers in androgen insensitivity syndrome (AIS)
Complete Androgen Insensitivity Syndrome: A Rare Case of Prenatal Diagnosis
Metabolic effects of estradiol versus testosterone in complete androgen insensitivity syndrome
Intronic PRRT2 mutation generates novel splice acceptor site and causes paroxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC) in a three generation family
Clinical, hormonal and genetic characteristics of androgen insensitivity syndrome in 39 Chinese patients
Challenges in clinical and laboratory diagnosis of androgen insensitivity syndrome: a case report
Embryonal carcinoma in androgen insensitivity syndrome
Androgen responsive intronic non-coding RNAs
Bilateral Breast Phyllodes Tumor in Androgen Insensitivity Syndrome
LINE1-mediated epigenetic repression of androgen receptor transcription causes androgen insensitivity syndrome
Two cases of androgen insensitivity due to somatic mosaicism
Complete Androgen Insensitivity Syndrome: Role of Imaging for Diagnosis
Genome-wide screening of biomarkers in androgen insensitivity syndrome (AIS)
Complete Androgen Insensitivity Syndrome: A Rare Case of Prenatal Diagnosis
Metabolic effects of estradiol versus testosterone in complete androgen insensitivity syndrome
Intronic PRRT2 mutation generates novel splice acceptor site and causes paroxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC) in a three generation family
Clinical, hormonal and genetic characteristics of androgen insensitivity syndrome in 39 Chinese patients
Challenges in clinical and laboratory diagnosis of androgen insensitivity syndrome: a case report
Embryonal carcinoma in androgen insensitivity syndrome
Androgen responsive intronic non-coding RNAs
Bilateral Breast Phyllodes Tumor in Androgen Insensitivity Syndrome
LINE1-mediated epigenetic repression of androgen receptor transcription causes androgen insensitivity syndrome
Two cases of androgen insensitivity due to somatic mosaicism
Complete Androgen Insensitivity Syndrome: Role of Imaging for Diagnosis
Genome-wide screening of biomarkers in androgen insensitivity syndrome (AIS)
Complete Androgen Insensitivity Syndrome: A Rare Case of Prenatal Diagnosis
Metabolic effects of estradiol versus testosterone in complete androgen insensitivity syndrome
Intronic PRRT2 mutation generates novel splice acceptor site and causes paroxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC) in a three generation family
Clinical, hormonal and genetic characteristics of androgen insensitivity syndrome in 39 Chinese patients