Sindrom Rett (Indonesian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sindrom Rett" in Indonesian language version.

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Andrew S. Davis (25 October 2010). Handbook of Pediatric Neuropsychology. Springer Publishing Company. ISBN 082615736X. Rett initially called this syndrome cerebroaatrophic hyperammonemia, but the elevated ammonia levels in the bloodstream were later found to be only rarely associated with this condition (can Acker, Loncola, & Can Acker, 2005).

doi.org

Percy, Alan (2013–2015). "The American History of Rett Syndrome". Pediatric neurology. 50 (1). doi:10.1016/j.pediatrneurol.2013.08.018. ISSN 0887-8994. PMC 3874243 . PMID 24200039.
Amir, Ruthie; Van den Veyver, Ignatia; Wan, Mimi; Tran, Charles; Francke, Uta; Zoghbi, Huda (1999). "Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2". Nature Genetics. 23 (2): 185–8. doi:10.1038/13810. PMID 10508514.

nih.gov

ncbi.nlm.nih.gov

Rett A (September 1966). "[On a unusual brain atrophy syndrome in hyperammonemia in childhood]". Wien Med Wochenschr (dalam bahasa German). 116 (37): 723–6. PMID 5300597.
Percy, Alan (2013–2015). "The American History of Rett Syndrome". Pediatric neurology. 50 (1). doi:10.1016/j.pediatrneurol.2013.08.018. ISSN 0887-8994. PMC 3874243 . PMID 24200039.
Amir, Ruthie; Van den Veyver, Ignatia; Wan, Mimi; Tran, Charles; Francke, Uta; Zoghbi, Huda (1999). "Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2". Nature Genetics. 23 (2): 185–8. doi:10.1038/13810. PMID 10508514.

ghr.nlm.nih.gov

"Rett syndrome". Genetics Home Reference (dalam bahasa Inggris). December 2013. Diakses tanggal 14 October 2017.

ninds.nih.gov

"Rett Syndrome Fact Sheet". National Institute of Neurological Disorders and Stroke. Diakses tanggal 14 October 2017.

rarediseases.org

"Rett Syndrome". NORD (National Organization for Rare Disorders). 2015. Diakses tanggal 14 October 2017.

worldcat.org

Percy, Alan (2013–2015). "The American History of Rett Syndrome". Pediatric neurology. 50 (1). doi:10.1016/j.pediatrneurol.2013.08.018. ISSN 0887-8994. PMC 3874243 . PMID 24200039.