Modeling Fragile X Syndrome: Characterizing Fmr1 Gene Knockout Mice across Genotype, Behavior, and Morphology

Objective: Fragile X syndrome (FXS) is a hereditary condition resulting from dynamic mutations in the Fmr1 gene, leading to reduced or absent fragile X mental retardation protein (FMRP). Although molecular genetic diagnostics for FXS have advanced, there is currently a lack of effective clinical tre...

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Detaylı Bibliyografya
Asıl Yazarlar:	Yonghua Liao, Junjie Liu, Jinyuan Zhang, Da Chen, Yifan Liu, Zhuolin Li, Hao Su, Jiaye Tang, Shengqiang Chen
Materyal Türü:	Artigo
Dil:	Inglês
Baskı/Yayın Bilgisi:	Wolters Kluwer Medknow Publications 2024-09-01
Seri Bilgileri:	Neurological Sciences and Neurophysiology
Konular:	behavioral studies fmr1 fragile x mental retardation protein fragile x syndrome genotype morphology
Online Erişim:	https://journals.lww.com/10.4103/nsn.nsn_25_24
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Modeling Fragile X Syndrome: Characterizing Fmr1 Gene Knockout Mice across Genotype, Behavior, and Morphology

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