Загрузка...
Association of Mutations in SLC12A1 Encoding the NKCC2 Cotransporter With Neonatal Primary Hyperparathyroidism
CONTEXT: Primary hyperparathyroidism with hypercalciuria has not been described in the newborn period. OBJECTIVE: Our objectives are to identify the genetic basis for neonatal primary hyperparathyroidism in a family with 2 affected children. SUBJECTS: An African American boy presenting with mild neo...
Сохранить в:
| Опубликовано в: : | J Clin Endocrinol Metab |
|---|---|
| Главные авторы: | , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Endocrine Society
2016
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4870850/ https://ncbi.nlm.nih.gov/pubmed/26963954 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2016-1211 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|