Header Logo

Connection

EDWARD COOPER to Polymorphism, Single Nucleotide

Back to Details
This is a "connection" page, showing publications EDWARD COOPER has written about Polymorphism, Single Nucleotide.
EDWARD COOPER
Connection Strength
0.074
Polymorphism, Single Nucleotide
  1. Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H. Epilepsia. 2017 03; 58(3):436-445.
    View in: PubMed
    Score: 0.074
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.