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The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Finasteride helps female-pattern hair loss.

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

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

LIPH mutations cause woolly hair in some Chinese people.

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The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

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The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

ASLNC168501 may help treat hair loss by boosting hair follicle stem cell activity.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

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PNU 157706 is a more effective treatment than finasteride for conditions caused by DHT, like enlarged prostate and hair loss.

ASLNC168501 can help treat hair loss by restoring hair follicle stem cell function.