Human growth disorders associated with impaired GH action: Defects in STAT5B and JAK2
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Endocrinology,Molecular Biology,Biochemistry
Reference92 articles.
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2. Atypical GH Insensitivity Syndrome and Severe Insulin-Like Growth Factor-I Deficiency Resulting from Compound Heterozygous Mutations of the GH Receptor, Including a Novel Frameshift Mutation Affecting the Intracellular Domain
3. The structure of human STAT5A and B genes reveals two regions of nearly identical sequence and an alternative tissue specific STAT5B promoter;Ambrosio;Gene,2002
4. A dominant-negative mutation of the growth hormone receptor causes familial short stature;Ayling;Nat. Genet.,1997
5. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders;Baxter;Lancet,2005
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