[HTML] frontiersin.org

[HTML][HTML] MeCP2: the genetic driver of Rett syndrome epigenetics

KV Good, JB Vincent, J Ausió - Frontiers in Genetics, 2021 - frontiersin.org
Mutations in methyl CpG binding protein 2 (MeCP2) are the major cause of Rett syndrome
(RTT), a rare neurodevelopmental disorder with a notable period of developmental …
被引用次数：85 相关文章

MeCP2: The Genetic Driver of Rett Syndrome Epigenetics

KV Good, JB Vincent, J Ausió - Epigenetic Mechanisms and Their …, 2021 - books.google.com
Mutations in methyl CpG binding protein 2 (MeCP2) are the major cause of Rett syndrome
(RTT), a rare neurodevelopmental disorder with a notable period of developmental …

MeCP2: The Genetic Driver of Rett Syndrome Epigenetics

KV Good, JB Vincent, J Ausió - Frontiers in Genetics, 2021 - cir.nii.ac.jp
抄録< jats: p> Mutations in methyl CpG binding protein 2 (MeCP2) are the major cause of
Rett syndrome (RTT), a rare neurodevelopmental disorder with a notable period of …

MeCP2: The Genetic Driver of Rett Syndrome Epigenetics.

KV Good, JB Vincent, J Ausió - Frontiers in Genetics, 2021 - europepmc.org
Mutations in methyl CpG binding protein 2 (MeCP2) are the major cause of Rett syndrome
(RTT), a rare neurodevelopmental disorder with a notable period of developmental …
[HTML] nih.gov

[HTML][HTML] MeCP2: The Genetic Driver of Rett Syndrome Epigenetics

KV Good, JB Vincent, J Ausió - Frontiers in Genetics, 2021 - ncbi.nlm.nih.gov
Mutations in methyl CpG binding protein 2 (MeCP2) are the major cause of Rett syndrome
(RTT), a rare neurodevelopmental disorder with a notable period of developmental …

MeCP2: The Genetic Driver of Rett Syndrome Epigenetics

KV Good, JB Vincent, J Ausió - Frontiers in genetics, 2021 - pubmed.ncbi.nlm.nih.gov
Mutations in methyl CpG binding protein 2 (MeCP2) are the major cause of Rett syndrome
(RTT), a rare neurodevelopmental disorder with a notable period of developmental …