CYP21A2 Gene Mutations in Congenital Adrenal Hyperplasia: Genotype-phenotype correlation in Turkish children
Firdevs Baş, Hülya Kayserili, Feyza Darendelıler, Zehra Oya Uyguner, Hülya Günöz, Memnune Yüksel Apak, Fatmahan Atalar, Rüveyde Bundak, Robert C. Wilson, Maria I. New, Bernd Wollnik, Nurçin Saka
- ISSN / E-ISSN
- — / —
- DOI
- 10.4008/jcrpe.v1i3.49 ↗
- Volume · Issue · Pages
- 1 · 3 · 116-128
- Publisher
- Galenos Publishing House
- Article URL
- https://doi.org/10.4008/jcrpe.v1i3.49 ↗
- Article details
- Unverified
Publication date (each date has its type and source)
24 Apr 2009
OpenAlex publication date · source: OpenAlex
| Type | Date | Source |
|---|---|---|
| OpenAlex publication date | 24 Apr 2009 | OpenAlex |
Keywords (as given): congenital adrenal hyperplasia; 21-hydroxylase deficiency; genotype-phenotype correlation; Turkish children; salt wasting; exon 6 mutations
HEC Status at Publication Not the journal's current status
HEC Status at PublicationNot conclusive
Historical status could not be conclusively determined.
- HEC status cannot be determined for this date: no HEC list is recorded as in effect on it.
Best available information, not a definitive status: HEC status cannot be determined for this date: no HEC list is recorded as in effect on it.
- Journal
- JCRPE Journal of Clinical Research in Pediatric Endocrinology
- Publication date used
- 24 Apr 2009 (OpenAlex publication date)
- Applicable HEC period
- None recorded for this date
- Category
- —
- Recognition status
- Unknown (NO_PERIOD_FOR_DATE)
- Source
- —
- Verification status
- Not available
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