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

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

The document's conclusion cannot be determined.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

SQSTM1 gene issues may increase the risk of alopecia areata.

A unique gene mutation was found in a family with monilethrix.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The hr gene is linked to hair loss in Valle del Belice sheep.

The document's conclusion cannot be provided because the document cannot be parsed.

A new genetic variant of Woodhouse-Sakati syndrome was found in two adult sisters in Russia.

IL16 gene variations may affect the risk of alopecia areata in Koreans.

No significant link was found between the studied genes and female hair loss in the Polish population.

A new DSG4 gene mutation causes hair defects in a young girl.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

The study found genetic variations in sheep that affect traits like milk production, growth, and health.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

The document's conclusion cannot be provided as the content is not available.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.