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Connection

Debopam Samanta to Neuroaxonal Dystrophies

This is a "connection" page, showing publications Debopam Samanta has written about Neuroaxonal Dystrophies.

 
Connection Strength
  
 
 
1.495
  
  1. Samanta D, Ramakrishnaiah R, Frye RE. Complex Heterozygous Polymerase Gamma Mutation and Cerebral Folate Deficiency in a Child with Refractory Partial Status. Neurol India. 2022 Sep-Oct; 70(5):2265-2267.
    View in: PubMed
    Score: 0.842
  2. Samanta D, Ramakrishnaiah R, Frye RE. Complex heterozygous polymerase gamma mutation and cerebral folate deficiency in a child with refractory partial status. Neurol India. 2019 Jan-Feb; 67(1):259-260.
    View in: PubMed
    Score: 0.653
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.