Varaico: Literature-Extracted Genetic Variants

Gene:GH1
Variant:p.S97_N98Splc
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GH1

NM_000515.5:p.S97_N98Splc

Associated Papers

Growth hormone treatment outcomes in children with genetic isolated growth hormone deficiency.

Aouchiche K et al.

European Journal of Pediatrics, 2025

A Novel Variant in an Intron Splicing Enhancer Associated with Familial Growth Hormone Deficiency.

Radovick S et al.

Hormone Research in Paediatrics, 2025

Genetic variations, clinical presentation and treatment outcome of isolated growth hormone deficiency type I and II: case series and review of the literature.

Li R et al.

Endocrine, 2025

The clinical and genetic aspects of six individuals with GH1 variants and isolated growth hormone deficiency type II.

Huang X et al.

Frontiers in Endocrinology, 2024

39435354 (PubMed )
Supplement: Table1.docx

Evaluation of Bioinformatic Programmes for the Analysis of Variants within Splice Site Consensus Regions.

Tang R et al.

Advances in Bioinformatics, 2016

27313609 (PubMed )
Supplement: 5614058.f1.pdf

Interpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis.

Caminsky N et al.

F1000research, 2014

25717368 (PubMed )
Supplement: f1000research-3-6038-s0000.tgz › e0d3facd-5877-477e-9217-8c5aa68746f2_Supplementary-Tables-11112014.zip › Supplementary-Tables-and-Figures-11112014 › Supplementary_Table_10._Splicing_Mutation_Calculator_Source_Datav2.xlsx › Supplementary_Table_10

A novel IVS2 -2A>T splicing mutation in the GH-1 gene in familial isolated growth hormone deficiency type II in the spectrum of other splicing mutations in the Russian population.

Fofanova OV et al.

The Journal of Clinical Endocrinology and Metabolism, 2003

Genetic characterization of growth hormone deficiency and resistance: implications for treatment with recombinant growth hormone.

Baumann G

American Journal of Pharmacogenomics : Genomics-related Research in Drug Development and Clinical Practice, 2002

A novel splicing mutation in exon 4 (456G>A) of the GH1 gene in a patient with congenital isolated growth hormone deficiency.

Fofanova OV et al.

Hormones (athens, Greece), 0

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."