Identification of mutations in Iranian patients’ DAX-1 gene with X-linked adrenal hypoplasia congenital
Objective(s): X-linked adrenal hypoplasia congenital (X-linked AHC) is a rare disorder, characterized by infantile-onset acute primary adrenal insufficiency and hypogonadotropic hypogonadism (HH) at an average age of three weeks and onset in roughly 40% is in childhood. Its cause is an inactivating...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
SpringerOpen
2017-04-01
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| Series: | Egyptian Journal of Medical Human Genetics |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S1110863016300301 |