Immunology and Genetics
November 2009
in “
Medical & surgical dermatology
”
CYP19A1 gene female pattern hair loss PRKARIA gene Carney complex major histocompatibility complex keloid scarring TGM1 mutation acral self-healing collodion baby bcl-xL expression primary cutaneous follicle center lymphomas erythema nodosum sarcoidosis Vitamin D3 analogue natural killer T cells keloid scars collodion baby skin lymphomas Vitamin D3
Studysummary This study found that haploinsufficiency of SPINK5 can lead to Netherton syndrome when a single null mutation combines with homozygous G1258A polymorphisms, suggesting it acts as a genuine mutation affecting LEKTI function.
Automatically generated from the study's abstract, not written by a person, and not a review of the full paper. Not medical advice or a treatment recommendation. Read the original study, and consult a qualified healthcare professional before changing treatment. Full disclaimer
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