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Liu, D. LPAR6 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4435 (accessed on 29 September 2026).
Liu D. LPAR6 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4435. Accessed September 29, 2026.
Liu, Dean. "LPAR6 Gene" Encyclopedia, https://encyclopedia.pub/entry/4435 (accessed September 29, 2026).
Liu, D. (2020, December 23). LPAR6 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4435
Liu, Dean. "LPAR6 Gene." Encyclopedia. Web. 23 December, 2020.
LPAR6 Gene
Edit

Lysophosphatidic acid receptor 6

genes

References

  1. Azeem Z, Jelani M, Naz G, Tariq M, Wasif N, Kamran-Ul-Hassan Naqvi S, Ayub M, Yasinzai M, Amin-Ud-Din M, Wali A, Ali G, Chishti MS, Ahmad W. Novel mutations inG protein-coupled receptor gene (P2RY5) in families with autosomal recessivehypotrichosis (LAH3). Hum Genet. 2008 Jun;123(5):515-9. doi:10.1007/s00439-008-0507-7.
  2. Khan S, Habib R, Mir H, Umm-e-Kalsoom, Naz G, Ayub M, Shafique S, Yamin T, AliN, Basit S, Wasif N, Kamran-Ul-Hassan Naqvi S, Ali G, Wali A, Ansar M, Ahmad W.Mutations in the LPAR6 and LIPH genes underlie autosomal recessivehypotrichosis/woolly hair in 17 consanguineous families from Pakistan. Clin ExpDermatol. 2011 Aug;36(6):652-4. doi: 10.1111/j.1365-2230.2011.04014.x.
  3. Kurban M, Wajid M, Shimomura Y, Christiano AM. Mutations in LPAR6/P2RY5 andLIPH are associated with woolly hair and/or hypotrichosis. J Eur Acad DermatolVenereol. 2013 May;27(5):545-9. doi: 10.1111/j.1468-3083.2012.04472.x.
  4. Pasternack SM, von Kügelgen I, Al Aboud K, Lee YA, Rüschendorf F, Voss K,Hillmer AM, Molderings GJ, Franz T, Ramirez A, Nürnberg P, Nöthen MM, Betz RC. G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance ofhuman hair growth. Nat Genet. 2008 Mar;40(3):329-34. doi: 10.1038/ng.84.
  5. Shimomura Y, Wajid M, Ishii Y, Shapiro L, Petukhova L, Gordon D, ChristianoAM. Disruption of P2RY5, an orphan G protein-coupled receptor, underliesautosomal recessive woolly hair. Nat Genet. 2008 Mar;40(3):335-9. doi:10.1038/ng.100.
  6. Tariq M, Ayub M, Jelani M, Basit S, Naz G, Wasif N, Raza SI, Naveed AK, ullah Khan S, Azeem Z, Yasinzai M, Wali A, Ali G, Chishti MS, Ahmad W. Mutations in theP2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.Br J Dermatol. 2009 May;160(5):1006-10. doi: 10.1111/j.1365-2133.2009.09046.x.
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Update Date: 23 Dec 2020
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