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January 1, 1994Human Molecular Genetics

An additional family with Startle disease and a G1192A mutation at the α1 subunit of the inhibitory glycine receptor gene

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Authors

DSDaniel F. SchorderetInstitut de Recherche en OpthalmologieGPG PesciaUniversity of GenevaABAndrea BernasconiGarrahan Hospital

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Schorderet et al. (1994) studied this question.

synapsesocial.com/papers/6a9d7b79f54e3ef35f67ec2ehttps://doi.org/10.1093/hmg/3.7.1201
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