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Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome.

The American Journal of Human Genetics(2020)

Cited 40|Views46
Key words
ichthyosis follicularis,photophobia,atrichia,SREBF1,MBTPS2,sterol biosynthesis
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