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Phelan McDermid: Difference between revisions

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[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974951/pdf/fnsyn-10-00011.pdf Prospects of Zinc Supplementation in Autism Spectrum Disorders and Shankopathies Such as Phelan McDermid Syndrome]
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974951/pdf/fnsyn-10-00011.pdf Prospects of Zinc Supplementation in Autism Spectrum Disorders and Shankopathies Such as Phelan McDermid Syndrome]
 
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[[nl:Syndroom van Phelan-McDermid]]
[[nl:Syndroom van Phelan-McDermid]]

Latest revision as of 22:12, 25 September 2018

(PMS[1]) is a rare genetic condition caused by deletion of terminal end of chromosome 22[2] , about 44% of people develops seizures[3]

Prospects of Zinc Supplementation in Autism Spectrum Disorders and Shankopathies Such as Phelan McDermid Syndrome

References

References:
  1. ↑ https://www.ncbi.nlm.nih.gov/books/NBK1198/
  2. ↑ Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndromology
  3. ↑ DMSF
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