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Please use this identifier to cite or link to this item: https://doi.org/10.1111/cge.12680
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dc.titlePDGFRB mutation causes autosomal-dominant Penttinen syndrome
dc.contributor.authorAminkeng, F
dc.date.accessioned2022-12-01T08:33:53Z
dc.date.available2022-12-01T08:33:53Z
dc.date.issued2015-12-01
dc.identifier.citationAminkeng, 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
dc.identifier.issn0009-9163
dc.identifier.issn1399-0004
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/235098
dc.description.abstractA point mutation in PDGFRB causes autosomal-dominant Penttinen syndrome Johnston JJ et al. (2015) American Journal of Human Genetics 97(3): 465-474.
dc.language.isoen
dc.publisherWILEY-BLACKWELL
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectGenetics & Heredity
dc.typeArticle
dc.date.updated2022-11-30T18:48:26Z
dc.contributor.departmentMEDICINE
dc.description.doi10.1111/cge.12680
dc.description.sourcetitleCLINICAL GENETICS
dc.description.volume88
dc.description.issue6
dc.description.page531-U7
dc.published.statePublished
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