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The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

Gene differences affect finasteride side effects in men with hair loss.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

The visfatin GT genotype may increase the risk of Alopecia Areata.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Certain gene variations may increase the risk of hair loss in Egyptians.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

A specific gene mutation causes congenital hair loss.

LIPH mutations cause woolly hair in some Chinese people.

Pilomatricomas are often linked to genetic syndromes, especially Apert syndrome, and genetic analysis is crucial for diagnosis.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

A specific gene change is linked to severe hair loss.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

HLA-DRB5 and other genes may be linked to alopecia universalis.

YAP1 is important for skin regeneration and may affect skin disorder treatments.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

The KRTAP13-3 gene affects wool fibre diameter variability in Chinese Tan sheep.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

Mutations in the SNRPE gene cause hereditary hair loss.

A boy with GAPO syndrome had hair loss similar to male pattern baldness without hormone issues, possibly due to skin or blood vessel problems.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.