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The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

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

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

5% topical minoxidil improves hair density and quality in monilethrix patients.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

5% topical minoxidil improves hair density and quality in monilethrix patients.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Woolly hair is a rare genetic condition with no effective treatments.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

LDE225 is a promising skin-applied treatment for basal cell carcinoma with good skin penetration and effectiveness.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

A gene mutation in mice causes permanent hair loss and skin issues.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

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

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

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

Topical minoxidil helped an 8-year-old boy with a genetic hair disorder grow hair.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.