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A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

South African sheep breeds have diverse genes affecting traits like coat color, horn development, and wool quality.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

The EDAR gene greatly affects hair thickness in Asian populations.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

The gene HDC is important for the development of hair follicles in newborn mice.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

Mutations in the SNRPE gene cause hereditary hair loss.

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

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

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

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Variants on chromosome 10 affect hair thickness in Dazu black goats.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

A hereditary condition causes hair loss and twisted hair in some family members.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Certain genes influence the direction of hair whorls on the scalp.

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

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

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

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

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

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.