Nalaganje...
PRL Mutation Causing Alactogenesis: Insights Into Prolactin Structure and Function Relationships
CONTEXT: Isolated prolactin deficiency is a rare disorder manifesting as absence of puerperal lactation. We identified a 2-generation family with 3 women experiencing alactogenesis. OBJECTIVE: We hypothesized a heterozygous genetic mutation. METHODS: This was a family-based study. Two generations of...
Shranjeno v:
| izdano v: | J Clin Endocrinol Metab |
|---|---|
| Main Authors: | , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Oxford University Press
2021
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8277218/ https://ncbi.nlm.nih.gov/pubmed/33770166 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/clinem/dgab201 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|