Familial glucocorticoid deficiency type 2: a case report
about
Adrenal androgens and androgen precursors-definition, synthesis, regulation and physiologic actions.Impact of a novel homozygous mutation in nicotinamide nucleotide transhydrogenase on mitochondrial DNA integrity in a case of familial glucocorticoid deficiency.Neonatal presentation of familial glucocorticoid deficiency resulting from a novel splice mutation in the melanocortin 2 receptor accessory protein.
P2860
Familial glucocorticoid deficiency type 2: a case report
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Familial glucocorticoid deficiency type 2: a case report
@ast
Familial glucocorticoid deficiency type 2: a case report
@en
Familial glucocorticoid deficiency type 2: a case report
@nl
type
label
Familial glucocorticoid deficiency type 2: a case report
@ast
Familial glucocorticoid deficiency type 2: a case report
@en
Familial glucocorticoid deficiency type 2: a case report
@nl
prefLabel
Familial glucocorticoid deficiency type 2: a case report
@ast
Familial glucocorticoid deficiency type 2: a case report
@en
Familial glucocorticoid deficiency type 2: a case report
@nl
P2093
P2860
P356
P1476
Familial glucocorticoid deficiency type 2: a case report
@en
P2093
Leyla Akın
Mustafa Ali Akın
Mustafa Kendirici
P2860
P304
P356
10.4274/JCRPE.V2I3.122
P577
2010-08-06T00:00:00Z