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Connection

CHARUL GIJAVANEKAR to Spastic Paraplegia, Hereditary

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This is a "connection" page, showing publications CHARUL GIJAVANEKAR has written about Spastic Paraplegia, Hereditary.
CHARUL GIJAVANEKAR
Connection Strength
0.196
Spastic Paraplegia, Hereditary
  1. Biallelic Variants in the Ectonucleotidase ENTPD1 Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, and Spastic Paraplegia. Ann Neurol. 2022 08; 92(2):304-321.
    View in: PubMed
    Score: 0.196
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.