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Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome |
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Titel: |
Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome |
Auteur: |
Wang, Huijun Humbatova, Aytaj Liu, Yuanxiang Qin, Wen Lee, Mingyang Cesarato, Nicole Kortüm, Fanny Kumar, Sheetal Romano, Maria Teresa Dai, Shangzhi Mo, Ran Sivalingam, Sugirthan Motameny, Susanne Wu, Yuan Wang, Xiaopeng Niu, Xinwu Geng, Songmei Bornholdt, Dorothea Kroisel, Peter M. Tadini, Gianluca Walter, Scott D. Hauck, Fabian Girisha, Katta M. Calza, Anne-Marie Bottani, Armand Altmüller, Janine Buness, Andreas Yang, Shuxia Sun, Xiujuan Ma, Lin Kutsche, Kerstin Grzeschik, Karl-Heinz Betz, Regina C. Lin, Zhimiao |
Verschenen in: |
The American journal of human genetics |
Paginering: |
Jaargang 107 () nr. 1 pagina's 34-45 |
Jaar: |
2020 |
Inhoud: |
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Uitgever: |
American Society of Human Genetics |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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