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IL16 gene variations may affect the risk of alopecia areata in Koreans.

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

Two new gene mutations cause a rare hair disorder.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

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

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

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

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

No significant genetic link to alopecia areata was found in the Jordanian group.

New genes linked to male pattern baldness were found on chromosome 20p11.

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

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

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

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

Autoimmune reactions may cause both alopecia areata and HAM.

Certain IL-18 gene variations may increase the risk of alopecia areata.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

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

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

Hairless gene not strongly linked to baldness.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

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