Header Logo

Connection

NEIL HANCHARD to Germ-Line Mutation

Back to Details
This is a "connection" page, showing publications NEIL HANCHARD has written about Germ-Line Mutation.
NEIL HANCHARD
Connection Strength
0.025
Germ-Line Mutation
  1. Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel ?-subunit in a case of early-onset phenotype of Liddle syndrome. Cold Spring Harb Mol Case Stud. 2016 11; 2(6):a001255.
    View in: PubMed
    Score: 0.025
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.