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 |
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Pages (from-to) | 265-266 |
Number of pages | 2 |
Journal | Nature Genetics |
Volume | 40 |
Issue number | 3 |
DOIs | |
State | Published - Mar 2008 |
Externally published | Yes |