glrb Literature

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Gene Literature (1)

XB-GENEPAGE-1011733

Papers associated with glrb

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	Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease., Rees MI, Harvey K, Pearce BR, Chung SK, Duguid IC, Thomas P, Beatty S, Graham GE, Armstrong L, Shiang R, Abbott KJ, Zuberi SM, Stephenson JB, Owen MJ, Tijssen MA, van den Maagdenberg AM, Smart TG, Supplisson S, Harvey RJ., Nat Genet. July 1, 2006; 38 (7): 801-6.

Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease., Rees MI, Harvey K, Pearce BR, Chung SK, Duguid IC, Thomas P, Beatty S, Graham GE, Armstrong L, Shiang R, Abbott KJ, Zuberi SM, Stephenson JB, Owen MJ, Tijssen MA, van den Maagdenberg AM, Smart TG, Supplisson S, Harvey RJ., Nat Genet. July 1, 2006; 38 (7): 801-6.

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