A mouse Mecp2-null mutation causes neurological symptoms that mimic rett syndrome
作者： Jacky Guy , Brian Hendrich , Megan Holmes , Joanne E. Martin , Adrian Bird
DOI: 10.1038/85899
关键词:
摘要: … Rett syndrome (RTT) is an inherited neurodevelopmental disorder of females that occurs … Most RTT patients are heterozygous for mutations in the X-linked gene MECP2 (refs. 3–12), …
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