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New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

Researchers found 15 new genetic links to skin traits in Japanese women.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

EDA2R gene linked to hair loss.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

No significant genetic link to alopecia areata was found in the Jordanian group.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

The scraggly mutation causes hair loss and skin defects in mice.

Certain genetic variations are linked to hair loss in Mexican men.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

A rare EGFR mutation in newborns leads to severe health issues and early death.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

A specific gene mutation causes complete hair loss without other health issues.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

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

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Mutations in the KRT16 gene can cause skin and nail disorders.