Disentangling the roots of inherited hair disorders

Eli Sprecher

doi:10.1038/ng0308-265

Disentangling the roots of inherited hair disorders

Eli Sprecher^*

^*Corresponding author for this work

Technion-Israel Institute of Technology

Research output: Contribution to journal › Short survey › peer-review

6 Scopus citations

Abstract

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.

Original language	English
Pages (from-to)	265-266
Number of pages	2
Journal	Nature Genetics
Volume	40
Issue number	3
DOIs	https://doi.org/10.1038/ng0308-265
State	Published - Mar 2008
Externally published	Yes

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Disentangling the roots of inherited hair disorders

Abstract

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