Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia
Year: 1993
Type: article
Study design: Observational Study
Source: Nature Genetics
DOI: 10.1038/ng1293-351
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2027426248
