SLITRK1 (SLIT and NTRK like family member 1) هوَ بروتين يُشَفر بواسطة جين SLITRK1 في الإنسان.
الوظيفة
الأهمية السريرية
المراجع
قراءة متعمقة
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- Abelson JF، Kwan KY، O'Roak BJ، وآخرون (2005). "Sequence variants in SLITRK1 are associated with Tourette's syndrome". Science. ج. 310 ع. 5746: 317–20. doi:10.1126/science.1116502. PMID 16224024.
- Burton A (2006). "SLITRK1 trouble in Tourette's syndrome". Lancet Neurology. ج. 4 ع. 12: 801. doi:10.1016/S1474-4422(05)70242-8. PMID 16323357.
- Wendland JR، Kruse MR، Murphy DL (2006). "Functional SLITRK1 var321, varCDfs and SLC6A4 G56A variants and susceptibility to obsessive-compulsive disorder". Mol. Psychiatry. ج. 11 ع. 9: 802–4. doi:10.1038/sj.mp.4001848. PMID 16936762.
- Zuchner S، Cuccaro ML، Tran-Viet KN، وآخرون (2006). "SLITRK1 mutations in trichotillomania". Mol. Psychiatry. ج. 11 ع. 10: 887–9. doi:10.1038/sj.mp.4001865. PMID 17003809.
