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Disentangling the roots of inherited hair disorders

Nature Genetics volume 40, pages 265–266 (2008)Cite this article

Rare syndromes offer unique opportunities to gain insight into central physiological processes. By deciphering the genetic basis of two rare inherited diseases, two studies identify a key role for P2Y5, a G protein–coupled receptor, in hair follicle development.

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Figure 1: Deciphering the pathogenesis of inherited nonsyndromic forms of alopecias reveals pathways regulating hair development.

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Authors and Affiliations

  1. Department of Dermatology at the Rambam Health Care Campus and Rappaport Institute, Eli Sprecher is in the Laboratory of Molecular Dermatology, Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 31096, Israel. e_sprecher@rambam.health.gov.il,

    Eli Sprecher

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  1. Eli Sprecher
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Sprecher, E. Disentangling the roots of inherited hair disorders. Nat Genet 40, 265–266 (2008). https://doi.org/10.1038/ng0308-265

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