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- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Disease causing homozygous variants in the human hairless gene
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
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- So we have 20k dollars human like machines available but no new effective treatment for hairloss since finasteride :)
- Great news recently for people with hairloss!
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