Connection

REBECCA LITTLEJOHN to Movement Disorders

This is a "connection" page, showing publications REBECCA LITTLEJOHN has written about Movement Disorders.
Connection Strength

0.285
  1. Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly. Am J Hum Genet. 2023 03 02; 110(3):499-515.
    View in: PubMed
    Score: 0.175
  2. Gain-of-Function Mutations in RARB Cause Intellectual Disability with Progressive Motor Impairment. Hum Mutat. 2016 08; 37(8):786-93.
    View in: PubMed
    Score: 0.110
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.