Molecular basis of nonclassical steroid 21-hydroxylase deficiency detected by neonatal mass screening in Japan

Since 1989, neonatal mass screening for congenital adrenal hyperplasia (CAH) has been performed in Japan, and the frequency of the classical form of 21-hydroxylase deficiency was found to be nearly identical to that in other countries. However, it has not yet been determined whether our mass screeni...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	The journal of clinical endocrinology and metabolism 1997-07, Vol.82 (7), p.2350-2356
Hauptverfasser:	Tajima, T, Fujieda, K, Nakae, J, Toyoura, T, Shimozawa, K, Kusuda, S, Goji, K, Nagashima, T, Cutler, Jr, G B
Format:	Artikel
Sprache:	eng
Schlagworte:	17-alpha-Hydroxyprogesterone - blood Adrenal Hyperplasia, Congenital Adrenocorticotropic Hormone - pharmacology Base Sequence Humans Infant, Newborn Japan Mass Screening Mutation Pedigree Sensitivity and Specificity Steroid 21-Hydroxylase - genetics
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!