Novel compound heterozygous mutations of the growth hormone-releasing hormone receptor gene in a case of isolated growth hormone deficiency-Reference-Cited by-同舟云学术

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Novel compound heterozygous mutations of the growth hormone-releasing hormone receptor gene in a case of isolated growth hormone deficiency

Published:2013-08 Issue:4 Volume:23 Page:89-97
ISSN:1096-6374
Container-title:Growth Hormone & IGF Research
language:en
Short-container-title:Growth Hormone & IGF Research

Author:

Soneda Akiko,Adachi Masanori,Muroya Koji,Asakura Yumi,Takagi Masaki,Hasegawa Tomonobu,Inoue Hiroshi,Itakura Mitsuo

Publisher

Elsevier BV

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference40 articles.

1. Causes of short stature. A community study of children in Newcastle upon Tyne;Lacey;Lancet,1974

2. Utah Growth Study: growth standards and the prevalence of growth hormone deficiency;Lindsay;J. Pediatr.,1994

3. Prevalence and demographic features of childhood growth hormone deficiency in Belgium during the period 1986–2001;Thomas;Eur. J. Endocrinol.,2004

4. Prevalence of severe growth hormone deficiency;Vimpani;Br. Med. J.,1977

5. Molecular basis of familial growth hormone deficiency;Pérez Jurado;Horm. Res.,1994

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2. A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family;Frontiers in Endocrinology;2023-03-07

3. Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature;Endocrine Journal;2017

4. Identification of novel GHRHR and GH1 mutations in patients with isolated growth hormone deficiency;Growth Hormone & IGF Research;2016-08

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