Functional characterization of compound heterozygosity for...

Functional characterization of compound heterozygosity for GlyRα1 mutations in the startle disease hyperekplexia

Ruth Rea, Marina A. Tijssen, Colin Herd, Rune R. Frants, Dimitri M. Kullmann
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Volume:
16
Year:
2002
Language:
english
Pages:
11
DOI:
10.1046/j.1460-9568.2002.02054.x
File:
PDF, 1.25 MB
english, 2002
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