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Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Two new gene mutations cause a rare hair disorder.

Scientists discovered two versions of a new human hair keratin gene.

New genetic mutations causing hair loss were found in a Chinese family.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

Hairless gene not strongly linked to baldness.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

The hr gene is linked to hair loss in Valle del Belice sheep.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

Haplogroup X found in Altaian population supports Amerindian origin.

TH antibodies in vitiligo and AA patients recognize the same protein parts.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

A new gene mutation is linked to monilethrix in the studied family.

Certain gene variations may increase the risk and severity of alopecia areata.

No clear link between specific gene and hair loss in Mexican brothers.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.