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The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.
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December 2017 in “The Journal of Dermatology” A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.
CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.
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Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.
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