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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...
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| Publicado en: | J Clin Endocrinol Metab |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Oxford University Press
2021
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| Assuntos: | |
| Acceso en liña: | 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 |
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