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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Mutations in the SNRPE gene cause hereditary hair loss.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

No significant link was found between the studied genes and female hair loss in the Polish population.

DNMT3A is crucial for healthy skin and hair growth.

A new gene mutation causes a rare type of hair loss.

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

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Mutations in specific genes disrupt development of sweat glands, teeth, hair, skin, and nails in HED.

HLD10 can include increased body hair and Mongolian spots.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

Researchers found a new mutation causing total hair loss from birth.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

A new genetic variant in the EEF2K gene may contribute to polycystic ovary syndrome.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

New treatments targeting specific genes show promise for treating keratin disorders.

A specific mutation in PA-PLA1α causes abnormal hair growth.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

A genetic hair protein variant is more common in Japanese people and is inherited.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

DNA analysis can help tailor alopecia treatment.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.