Please use this identifier to cite or link to this item:
https://doi.org/10.1111/cge.12680
| Title: | PDGFRB mutation causes autosomal-dominant Penttinen syndrome | Authors: | Aminkeng, F | Keywords: | Science & Technology Life Sciences & Biomedicine Genetics & Heredity |
Issue Date: | 1-Dec-2015 | Publisher: | WILEY-BLACKWELL | Citation: | Aminkeng, F (2015-12-01). PDGFRB mutation causes autosomal-dominant Penttinen syndrome. CLINICAL GENETICS 88 (6) : 531-U7. ScholarBank@NUS Repository. https://doi.org/10.1111/cge.12680 | Abstract: | A point mutation in PDGFRB causes autosomal-dominant Penttinen syndrome Johnston JJ et al. (2015) American Journal of Human Genetics 97(3): 465-474. | Source Title: | CLINICAL GENETICS | URI: | https://scholarbank.nus.edu.sg/handle/10635/235098 | ISSN: | 0009-9163 1399-0004 |
DOI: | 10.1111/cge.12680 |
| Appears in Collections: | Staff Publications Elements |
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| Clinical Genetics - 2015 - Aminkeng - PDGFRB mutation causes autosomal‐dominant Penttinen syndrome.pdf | 120.58 kB | Adobe PDF | CLOSED | Published |
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