相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Myt1l safeguards neuronal identity by actively repressing many non-neuronal fates
Moritz Mall et al.
NATURE (2017)
Associations of the Intellectual Disability Gene MYT1L with Helix-Loop-Helix Gene Expression, Hippocampus Volume and Hippocampus Activation During Memory Retrieval
Agnieszka Kepa et al.
NEUROPSYCHOPHARMACOLOGY (2017)
A systematic review of genetic syndromes with obesity
Y. Kaur et al.
OBESITY REVIEWS (2017)
MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus
Patricia Blanchet et al.
PLOS GENETICS (2017)
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity
Nina De Rocker et al.
GENETICS IN MEDICINE (2015)
Early-onset obesity and paternal 2pter deletion encompassing the ACP1, TMEM18, and MYT1L genes
Martine Doco-Fenzy et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2014)
A new patient with a terminal de novo 2p25.3 deletion of 1.9 Mb associated with early-onset of obesity, intellectual disabilities and hyperkinetic disorder
Maria Clara Bonaglia et al.
MOLECULAR CYTOGENETICS (2014)
MYT1L is a Candidate Gene for Intellectual Disability in Patients With 2p25.3 (2pter) Deletions
Servi J. C. Stevens et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2011)
分享论文
