טוען...
A Comprehensive Review of Genetically Engineered Mouse Models for Prader-Willi Syndrome Research
Prader-Willi syndrome (PWS) is a neurogenetic multifactorial disorder caused by the deletion or inactivation of paternally imprinted genes on human chromosome 15q11-q13. The affected homologous locus is on mouse chromosome 7C. The positional conservation and organization of genes including the impri...
שמור ב:
| הוצא לאור ב: | Int J Mol Sci |
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| Main Authors: | , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
MDPI
2021
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8037846/ https://ncbi.nlm.nih.gov/pubmed/33807162 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22073613 |
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