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Fig. 3 | BMC Endocrine Disorders

Fig. 3

From: Reporting a novel growth hormone receptor gene variant in an Iranian consanguineous pedigree with Laron syndrome: a case report

Fig. 3

Schematic representation of reported variants in the GHR gene and the corresponding protein structure including the signal peptide, an extracellular domain consisting of two FN3 subdomains, a transmembrane domain, and an intracellular domain. The identified variant in this study was marked in red [2,3,4,5,6, 8, 12, 13, 15, 17,18,19, 21, 23, 26,27,28,29, 31, 34, 36, 37, 43, 47, 48, 50, 51, 54,55,56, 58,59,60, 64, 65, 68,69,70, 72,73,74]

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BMC Endocrine Disorders

ISSN: 1472-6823

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