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Results 1 - 1 of 1 for "22q13.3" deletion syndrome
  1. SHANK3 gene 
    ... between neurons. The characteristic signs and symptoms of 22q13.3 deletion syndrome, which is also commonly known as Phelan-McDermid ... is responsible for many of the features of 22q13.3 deletion syndrome. A decrease in the functioning of synapses and ...
    https://medlineplus.gov/genetics/gene/shank3 - Genetics