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Identification of novel candidate pathogenic genes in pituitary stalk interruption syndrome by whole‐exome sequencing
Pituitary stalk interruption syndrome (PSIS) is a type of congenital malformation of the anterior pituitary, which leads to isolated growth hormone deficiency or multiple hypothalamic‐pituitary deficiencies. Many genetic factors have been explored, but they only account for a minority of the genetic...
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| Veröffentlicht in: | J Cell Mol Med |
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| Hauptverfasser: | , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
John Wiley and Sons Inc.
2020
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7579688/ https://ncbi.nlm.nih.gov/pubmed/32864857 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.15781 |
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