Jeffrey Kornitzer

2PUBLICATIONS
0CO-AUTHORS
Neurology and neuromuscular diseasesNeonatology
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Publications (2)

|Oct 24, 2018
A novel intronic homozygous mutation in the AMT gene of a patient with nonketotic hyperglycinemia and hyperammonemia.

Sarah Silverstein, Aravindhan Veerapandiyan, Caroline Hayes-Rosen

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