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Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions
Patients with Kallmann syndrome (KS) have hypogonadotropic hypogonadism caused by a deficiency of gonadotropin-releasing hormone (GnRH) and a defective sense of smell related to olfactory bulb aplasia. Based on the findings in a fetus affected by the X chromosome–linked form of the disease, it has b...
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| Main Authors: | , , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
American Society for Clinical Investigation
2010
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2947242/ https://ncbi.nlm.nih.gov/pubmed/20940512 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI43699 |
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