Novel human pathological mutations. Gene symbol: NR3C1. Disease: glucocorticoid receptor deficiency

Pretorius, C., McMahon, S. K., Ungerer, J. P., Salmon, N., Conwell, L. S. and Batch, J. A. (2009) Novel human pathological mutations. Gene symbol: NR3C1. Disease: glucocorticoid receptor deficiency. Human Genetics, 126 2: 337-337.

Author Pretorius, C.
McMahon, S. K.
Ungerer, J. P.
Salmon, N.
Conwell, L. S.
Batch, J. A.
Title Novel human pathological mutations. Gene symbol: NR3C1. Disease: glucocorticoid receptor deficiency
Journal name Human Genetics   Check publisher's open access policy
ISSN 0340-6717
1432-1203
Publication date 2009-08-01
Sub-type Article (original research)
Open Access Status Not yet assessed
Volume 126
Issue 2
Start page 337
End page 337
Total pages 1
Place of publication Germany
Publisher Springer
Q-Index Code CX
Q-Index Status Provisional Code
Institutional Status Non-UQ

Document type: Journal Article
Sub-type: Article (original research)
Collections: Mater Health Services Publications
School of Medicine Publications
 
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Created: Sat, 14 Jan 2017, 01:42:15 EST by Dr Louise Conwell on behalf of Mater Clinical Unit