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A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

A girl had rickets due to a gene mutation affecting vitamin D response.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

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

The rs1128977 gene variant may affect cholesterol and body measurements.

The MTR gene affects wool quality and production in Chinese Merino sheep.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

CT60 polymorphism might increase the risk of Alopecia Areata.

Certain gene variations are found in people with polycystic ovary syndrome.

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

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

A genetic marker linked to a type of hair loss was found in most patients studied.

A genetic variant in the KRT25 gene causes tightly curled hair.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

Genetic differences affect COVID-19 severity and treatment effectiveness.

Two genetic variations in Moa buffalo help them adapt to heat.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Longer CAG repeats in gene linked to more severe hair loss in females.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

A new gene mutation causes insulin resistance in a girl and her mother.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

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

A new mutation in the KRT86 gene causes a hair disorder with variable expression.