Your search for "ahi1" returned 727 TaqMan® SNP Genotyping Assays
Abelson helper integration site 1
This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]
1700015F03RIK, AHI-1, AHI1, D10BWG0629E, DJ71N10.1, JBTS3, ORF1
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