טוען...

A newly characterized AT-hook domain in MeCP2 determines clinical course of Rett syndrome and related disorders

Mutations in the X-linked MECP2 cause Rett syndrome, a devastating neurological disorder typified by a period of apparently normal development followed by loss of cognitive and psychomotor skills. Data from rare male patients suggest symptom onset and severity can be influenced by the location of th...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
Main Authors: Baker, Steven Andrew, Chen, Lin, Wilkins, Angela Dawn, Yu, Peng, Lichtarge, Olivier, Zoghbi, Huda Yahya
פורמט: Artigo
שפה:Inglês
יצא לאור: 2013
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC3641682/
https://ncbi.nlm.nih.gov/pubmed/23452848
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2013.01.038
תגים: הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!