Clinical phenotype of a Kallmann syndrome patient with IL17RD and CPEB4 variants
BackgroundThis study aimed to characterize the clinical phenotype and genetic variations in patients with Kallmann syndrome (KS).MethodsThis study involved the collection and analysis of clinical data from an individual with sporadic KS. Following this, peripheral blood samples were obtained from th...
I tiakina i:
| Ngā kaituhi matua: | , , , , , |
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| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
Frontiers Media S.A.
2024-04-01
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| Rangatū: | Frontiers in Endocrinology |
| Ngā marau: | |
| Urunga tuihono: | https://www.frontiersin.org/articles/10.3389/fendo.2024.1343977/full |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
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