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

Cantú syndrome is caused by mutations in the ABCC9 gene.

New mutations in the hairless gene may cause hair loss and affect bone development.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

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

A specific gene mutation causes congenital hair loss.

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

Mutations in the hairless gene cause a rare form of permanent hair loss.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A specific gene change in APCDD1 increases the risk of hair loss.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

KATP channels are important for energy balance and are targeted by drugs for diabetes, hypoglycemia, hypertension, and hair loss.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A new mutation in the HR gene causes hair loss in a specific family.

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

All Indian dromedary camel breeds have the same KRTAP7 gene affecting hair quality.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Mutations in the SNRPE gene cause hereditary hair loss.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

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

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

A specific gene mutation causes complete hair loss in an Irish Traveller family.