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- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Woolly hair nevus
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- The twisting tale of woolly hair: a trait with many causes
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- A rare case of woolly hair with unusual associations
- Prevalent founder mutation c.736T>A of <i>LIPH</i> in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
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