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The Central Domain of MCPH1 Controls Development of the Cerebral Cortex and Gonads in Mice
MCPH1 is the first gene identified to be responsible for the human autosomal recessive disorder primary microcephaly (MCPH). Mutations in the N-terminal and central domains of MCPH1 are strongly associated with microcephaly in human patients. A recent study showed that the central domain of MCPH1, w...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9455054/ https://www.ncbi.nlm.nih.gov/pubmed/36078123 http://dx.doi.org/10.3390/cells11172715 |