Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome.
The American Journal of Human Genetics(2020)
Key words
ichthyosis follicularis,photophobia,atrichia,SREBF1,MBTPS2,sterol biosynthesis
AI Read Science
Must-Reading Tree
Example

Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined