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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

Androgenetic alopecia may cause schizophrenia, but schizophrenia does not cause androgenetic alopecia.

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

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Bcl-2 affects hair growth and pigmentation by controlling cell death.

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

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

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

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

PAON shows skin patterns due to genetic mosaicism.

HLD10 can include increased body hair and Mongolian spots.

Ets2 gene is crucial for placental development in mice.

Mutation in hairless gene may increase hair loss risk.

Certain genes may be linked to autoimmune conditions in people with alopecia areata.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Mutation in hairless gene may increase hair loss risk.

Male pattern hair loss may have evolved to promote younger fathers for offspring health and survival, encouraging monogamy and paternal nurturing.

Hairless gene not strongly linked to baldness.

Thyroid issues can cause alopecia areata.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

A new gene mutation causes a rare type of hair loss.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.