Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease - Concepedia

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Publication | Open Access

Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease

DOI Full Paper Access

232

Citations

25

References

2006

Year

Mark I. Rees, Kirsten Harvey, Brian R. Pearce, Seo‐Kyung Chung, Ian Duguid, P K Thomas, Sarah Beatty, Gail E. Graham, Linlea Armstrong, Rita Shiang,

Nature Genetics

Developmental BiologyMendelian DisorderHuman Startle DiseasePresynaptic ComponentGeneticsGenetic DisorderMolecular GeneticsDisease Gene IdentificationMolecular NeurobiologyMedicineNeurogenetics

References

	Year	Citations

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