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A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

A specific gene variant may increase the risk of developing Alopecia Areata.

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.

A new DSG4 gene mutation causes hair defects in a young girl.

A truncated protein linked to breast cancer may change cell adhesion.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

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

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A unique gene mutation was found in a family with monilethrix.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

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

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

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

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

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

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

Cutaneous lupus patients have higher levels of certain immune cells in their blood and skin.

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