Mutations in GH1 gene and isolated growth hormone deficiency (IGHD): A familial case of IGHD type I and systematic review

Author:

Li Qiuyue,Xu Zhenran,Zhang Miaoying,Zhao Zhuhui,Sun Bijun,Yang Lin,Lu Wei,Luo Feihong,Sun Chengjun

Publisher

Elsevier BV

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference32 articles.

1. Molecular basis for familial isolated growth hormone deficiency;Phillips;Proc. Natl. Acad. Sci. U. S. A.,1981

2. Genetic causes and treatment of isolated growth hormone deficiency-an update;Alatzoglou;Nat. Rev. Endocrinol.,2010

3. Growth hormone antibodies in patients treated with different preparations of human growth hormone (HGH);Illig;J. Clin. Endocrinol. Metab.,1970

4. Heterogeneous growth hormone (GH) gene mutations in familial GH deficiency;Cogan;J. Clin. Endocrinol. Metab.,1993

5. Autosomal dominant growth hormone (GH) deficiency type II: the Del32-71-GH deletion mutant suppresses secretion of wild-type GH;Lee;Endocrinology,2000

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