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JAMA Neurology
|
October 9, 2013
COX10 mutations resulting in complex multisystem mitochondrial disease that remains stable into adulthood
Robert D S Pitceathly, Jan-Willem Taanman, Shamima Rahman, et al.
Brain : a Journal of Neurology
|
November 21, 2013
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2
A Reghan Foley, Manoj P Menezes, Amelie Pandraud, et al.
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of 30
Search research articles
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Showing results (291-300 of 292) with videos related to
Sort By:
Page
of 30
You have reached the last page of results.
This site can display upto 292 results.
JAMA Neurology
|
October 9, 2013
COX10 mutations resulting in complex multisystem mitochondrial disease that remains stable into adulthood
Robert D S Pitceathly, Jan-Willem Taanman, Shamima Rahman, et al.
Brain : a Journal of Neurology
|
November 21, 2013
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2
A Reghan Foley, Manoj P Menezes, Amelie Pandraud, et al.
Page
of 30