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Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor / Mark Rees, Mark Andrew, Saeed Jawad, Mike J Owen

Human Molecular Genetics, Volume: 3, Issue: 12, Pages: 2175 - 2179

Swansea University Author: Mark Rees

Published in: Human Molecular Genetics
Published: 1994
URI: https://cronfa.swan.ac.uk/Record/cronfa20917
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College: Swansea University Medical School
Issue: 12
Start Page: 2175
End Page: 2179