MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patients-Reference-Cited by-同舟云学术

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MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patients

Published:2006-06 Issue:5 Volume:28 Page:305-310
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Moog Ute,Roozendaal Kees Van,Smeets Eric,Tserpelis Demis,Devriendt Koen,Buggenhout Griet Van,Frijns Jean-Pierre,Schrander-Stumpel Connie

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference44 articles.

1. An update on clinically applicable diagnostic criteria in rett syndrome. Comments to rett syndrome clinical criteria consensus panel satellite to European paediatric neurology society meeting, baden baden, Germany, 11 September 2001;Hagberg;Eur J Paediatr Neurol,2002

2. Rett syndrome: clinical peculiarities and biological mysteries;Hagberg;Acta Paediatr,1995

3. Rett syndrome is caused by mutations in X-linked MeCP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999

4. Rett syndrome in adolescent and adult females: clinical and molecular genetic findings;Smeets;Am J Med Genet,2003

5. Phenotypic manifestations of MECP2 mutations in classical and atypical rett syndrome;Schanen;Am J Med Genet,2004

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. MECP2-Related Disorders in Males;International Journal of Molecular Sciences;2021-09-04

2. MECP2-related conditions in males: A systematic literature review and 8 additional cases;European Journal of Paediatric Neurology;2021-09

3. Copy number variation in genetic epilepsy with febrile seizures plus;European Journal of Paediatric Neurology;2020-07

4. MeCP2 Dysfunction in Rett Syndrome and Neuropsychiatric Disorders;Methods in Molecular Biology;2019

5. The array of clinical phenotypes of males with mutations in Methyl‐CpG binding protein 2;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2018-12-07

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