All individuals with variants in gene CST6

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00466712 FamPatII2 PubMed: Eckl 2021 3-generation family, affected mother/son F - Austria - - - - - KFSD see paper; ..., generalised follicular hyperkeratosis, dry skin, scarring alopecia scalp, sparse eyebrows, sparse eyelashes, occipital folliculitis, hypohidrosis, myopia, astigmatism 1 2 Johan den Dunnen
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