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 (Q28235848)
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scientific article (publication date: December 1994)
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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 |
scientific article (publication date: December 1994) |
Statements
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 (English)
M Andrew
S Jawad
1 December 1994
Identifiers
2 references
2 references