![]() |
Identification of a novel point mutation in DAX-1 gene in a patient with adrenal hypoplasia congenita
Han Saem Choi, Ahreum Kwon, Hyun Wook Chae, Junghwan Suh, Kyung Chul Song, Jin-Sung Lee, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2021;26(2):126-129. Published online 2021 Jun 30 DOI: https://doi.org/10.6065/apem.2040088.044
|
Citations to this article as recorded by
A novel variant in NR0B1 causing X-linked adrenal hypoplasia congenita
Seung Heo, Young Suk Shim, Hae Sang Lee, Jin Soon Hwang
Annals of Pediatric Endocrinology & Metabolism.2024; 29(3): 204. CrossRef Neglected Adrenal Hypoplasia Congenita in Two Siblings with Novel Genetic Mutations in NR0B1 Gene and Notable Clinical Course: A Case Report
Shayesteh Khalili, Anahita Zakeri, Farzad Hadaegh, Seyed Saeed Tamehri Zadeh
Endocrine, Metabolic & Immune Disorders - Drug Targets.2024; 24(14): 1704. CrossRef A rare variant of DAX1 mutation presenting with primary adrenal insufficiency and hypogonadotropic hypogonadism
Konsam Biona Devi, Mintu Mani Baruah, Trupti Prasad Nagendra, Sadam Hussain, Sanjay Kumar Bhadada, Rama Walia
IJEM Case Reports.2024; 2(4): 121. CrossRef Treatment of congenital hypogonadotropic hypogonadism in male patients
Hae Sang Lee, Young Suk Shim, Jin Soon Hwang
Annals of Pediatric Endocrinology & Metabolism.2022; 27(3): 176. CrossRef Growth alterations in rare forms of primary adrenal insufficiency: a neglected issue in paediatric endocrinology
Rosario Ferrigno, Daniela Cioffi, Valeria Pellino, Maria Cristina Savanelli, Antonella Klain
Endocrine.2022; 80(1): 1. CrossRef
|