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The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

Whale genes show changes that help them live in water, like less hair and better flippers.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Mutations in hKAP1 genes may cause hereditary hair disorders.

Low ERCC3 gene activity is linked to non-pigmented hair growth.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

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

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

KRTAP6 genes affect wool quality in sheep.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

The Thai version of the Family Dermatology Life Quality Index is a reliable and valid tool for assessing the quality of life of patients' families.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

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

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

Researchers found a gene mutation responsible for a rare hair loss condition.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The B2 genes are crucial for hair growth in rats.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Baldness is common in Korean men (60.5%), and those with a family history are 3.1 times more likely to have hairline recession.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.