Acquired microcephaly, regression of milestones, mitochondrial dysfunction, and episodic rigidity in a 46,XY male with a de novo MECP2 gene mutation.
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Identification and Treatment of Pathophysiological Comorbidities of Autism Spectrum Disorder to Achieve Optimal Outcomes.Neuropathological Mechanisms of Seizures in Autism Spectrum DisorderPrimary Mitochondrial Disease and Secondary Mitochondrial Dysfunction: Importance of Distinction for Diagnosis and TreatmentGastrointestinal dysfunction in autism spectrum disorder: the role of the mitochondria and the enteric microbiome.Treatments for biomedical abnormalities associated with autism spectrum disorder.Using the neurofibromatosis tumor predisposition syndromes to understand normal nervous system development.Autism, Mitochondria and Polybrominated Diphenyl Ether Exposure.Brief report: systematic review of Rett syndrome in males.Folate metabolism abnormalities in autism: potential biomarkers.Mitochondrial disease in 22q13 duplication syndrome.Autistic Siblings with Novel Mutations in Two Different Genes: Insight for Genetic Workups of Autistic Siblings and Connection to Mitochondrial Dysfunction.A novel mutation R190H in the AT-hook 1 domain of MeCP2 identified in an atypical Rett syndrome.
P2860
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P2860
Acquired microcephaly, regression of milestones, mitochondrial dysfunction, and episodic rigidity in a 46,XY male with a de novo MECP2 gene mutation.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Acquired microcephaly, regress ...... a de novo MECP2 gene mutation.
@en
type
label
Acquired microcephaly, regress ...... a de novo MECP2 gene mutation.
@en
prefLabel
Acquired microcephaly, regress ...... a de novo MECP2 gene mutation.
@en
P2093
P2860
P356
P1476
Acquired microcephaly, regress ...... a de novo MECP2 gene mutation.
@en
P2093
John Condie
Joshua Goldstein
Mark S Wainwright
P2860
P304
P356
10.1177/0883073809342004
P577
2010-02-08T00:00:00Z