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MCHR2 gene duplications may be linked to alopecia areata.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

A new gene mutation linked to a skin condition was found in a Spanish family.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

CAG repeat polymorphism and prostate zone volume are not reliable markers of long-term androgen sensitivity.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Genetic variants in specific genes cause a type of hair loss.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

TRPV3 gene mutations cause Olmsted syndrome symptoms, but severity varies.

Certain gene variations may increase the risk of hair loss in Egyptians.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

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

KAP8.1 gene variations affect cashmere weight in Inner Mongolian goats.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

A genetic variant in goats is linked to cashmere growth.

The TT genotype of a specific SNP in sheep is linked to better wool quality.