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The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

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Errors found in identifying furosemide and finasteride polymorphs due to incomplete data.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

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A new method accurately measures molecular movement without complex modeling.

Two new gene mutations cause a rare hair disorder.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

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Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

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Robertsonian translocation can cause recurrent miscarriages.

MK-0773 is a moderate inhibitor of the SRD5A2 enzyme.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

ESR2 gene linked to female-pattern hair loss.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

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

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

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