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(Created page with "(PMS) is a rare genetic condition caused by deletion of terminal end of chromosome 22<ref>Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndrom...")
 
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(PMS) is a rare genetic condition caused by deletion of terminal end of chromosome 22<ref>Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndromology</ref> , about 44% of people develops [[epilepsy|seizures]]<ref>DMSF</ref>
(PMS) is a rare genetic condition caused by deletion of terminal end of chromosome 22<ref>Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndromology</ref> , about 44% of people develops [[epilepsy|seizures]]<ref>DMSF</ref>
[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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Revision as of 13:16, 24 September 2018

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

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

  1. Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndromology
  2. DMSF