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A missense mutation of human Gephyrin (GPHN) is associated with Hyperekplexia and transcript isoform analysis re-defines the genomic structure of GPHN. / Mark Rees, Kristin Baer, Hamish Ward, Sharon Coleman, Luc Evans, Jan Miller, Henry Waldvogel, Richard Faull, Mike Owen, Russell Snell

AMERICAN JOURNAL OF HUMAN GENETICS, Volume: 69, Issue: 4, Pages: 627 - 628

Swansea University Author: Mark Rees

Published in: AMERICAN JOURNAL OF HUMAN GENETICS
Published: 2001
URI: https://cronfa.swan.ac.uk/Record/cronfa38449
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College: Swansea University Medical School
Issue: 4
Start Page: 627
End Page: 628