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MA Derr
OpenAlex ID:
A5043588669
A Novel Y332C Missense Mutation in the Intracellular Domain of the Human Growth Hormone Receptor (GHR) Does Not Alter STAT5b Signaling: Redundancy of GHR Intracellular Tyrosines Involved in STAT5b Signaling.
2010
·
MA Derr
, P Fang
, et al.
·
The Endocrine Society's 92nd Annual Meeting, June 19–22, 2010 - San Diego
·
5
Severe Short Stature Caused by Novel Compound Heterozygous Mutations of the Insulin-Like Growth Factor 1 Receptor.
2010
·
P Fang
, YH Cho
, et al.
·
The Endocrine Society's 92nd Annual Meeting, June 19–22, 2010 - San Diego
·
1
A Novel Heterozygous STAT5b Variant, N160S, Associated with Modest Short Stature.
2010
·
V Hwa
, NE Friedman
, et al.
·
The Endocrine Society's 92nd Annual Meeting, June 19–22, 2010 - San Diego
A Case of Severe IGF-1 Deficiency Secondary to a Novel Homozygous Deletion in the Growth Hormone Receptor (GHR) Gene.
2010
·
D Koltin
, MA Derr
, et al.
·
The Endocrine Society's 92nd Annual Meeting, June 19–22, 2010 - San Diego
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Works count:
4
Citation count:
6
H-index:
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