An additional family with Startle disease and a G1192A mutation at the alpha 1 subunit of the inhibitory glycine receptor gene.
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Schorderet DF, Pescia G, Bernasconi A, Regli F
An additional family with Startle disease and a G1192A mutation at the alpha 1 subunit of the inhibitory glycine receptor gene.
Hum Mol Genet. 1994 Jul;3(7):1201.
- PubMed ID
- 7981700 [ View in PubMed]
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