A clinical case–control comparison of epidermal innervation density in Rett syndrome

INTRODUCTION: Rett syndrome (RTT), a rare neurodevelopmental disorder occurring primarily in females (1:10–15,000 female live births), is most often caused by loss‐of‐function mutations in the X‐linked methyl‐CpG‐binding protein 2 gene (MECP2). Clinical observations and preclinical findings indicate...

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Detalhes bibliográficos
Publicado no:Brain Behav
Main Authors: Symons, Frank J., Barney, Chantel C., Byiers, Breanne J., McAdams, Brian D., Foster, Shawn X. Y. L., Feyma, Timothy J., Wendelschafer‐Crabb, Gwen, Kennedy, William R.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2019
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Original Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6520294/
https://ncbi.nlm.nih.gov/pubmed/30980517
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/brb3.1285
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