The New England journal of medicine | 2019

Phenotype in an Infant with SOD1 Homozygous Truncating Mutation.

 
 
 
 
 
 
 
 
 
 

Abstract


Absence of SOD1 Activity and Motor Neuron Syndrome In a child with a homozygous truncating mutation in SOD1, SOD1 activity in red cells was absent and fibroblasts grew only with oxygen deprivation....

Volume None
Pages None
DOI 10.1056/NEJMc1905039
Language English
Journal The New England journal of medicine

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