| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8476576 | Molecular and Cellular Endocrinology | 2018 | 7 Pages |
Abstract
These cases of rare subtypes of CAH illustrate the heterogeneous phenotypic and genetic features of these subtypes and add unique novel mutations to the previously known ones.
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Authors
Meshael M. Alswailem, Ohoud S. Alzahrani, Doha S. Alhomaidah, Rahma Alasmari, Ebtesam Qasem, Avaniyapuram Kannan Murugan, Afaf Alsagheir, Imad Brema, Bassam Ben Abbas, Mohammed Almehthel, Ali Almeqbali, Ali S. Alzahrani,