Novel Variant in PLAG1 in a Familial Case with Silver-Russell Syndrome Suspicion.
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| Title: | Novel Variant in PLAG1 in a Familial Case with Silver-Russell Syndrome Suspicion. |
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| Authors: | Vado Y; Rare Diseases Research Group, Molecular (Epi) Genetics Laboratory, Bioaraba Health Research Institute, Araba University Hospital-Txagorritxu, Vitoria-Gasteiz, 01009 Araba, Spain.; NanoBioCel Research Group, Laboratory of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, Universidad del País Vasco/Euskal Herriko Unibertsitatea (UPV/EHU), Vitoria-Gasteiz, 01006 Araba, Spain., Pereda A; Rare Diseases Research Group, Molecular (Epi) Genetics Laboratory, Bioaraba Health Research Institute, Araba University Hospital-Txagorritxu, Vitoria-Gasteiz, 01009 Araba, Spain., Llano-Rivas I; Service of Genetics, BioCruces Health Research Institute, Hospital Universitario Cruces, Barakaldo, 48903 Bizkaia, Spain., Gorria-Redondo N; Service of Paediatric Neurology, Araba University Hospital, Vitoria-Gasteiz, 01009 Araba, Spain., Díez I; Department of Pediatric Endocrinology, Bioaraba Health Research Institute, Araba University Hospital-Txagorritxu, 01009 Vitoria-Gasteiz, Spain., Perez de Nanclares G; Rare Diseases Research Group, Molecular (Epi) Genetics Laboratory, Bioaraba Health Research Institute, Araba University Hospital-Txagorritxu, Vitoria-Gasteiz, 01009 Araba, Spain. |
| Source: | Genes [Genes (Basel)] 2020 Dec 05; Vol. 11 (12). Date of Electronic Publication: 2020 Dec 05. |
| Publication Type: | Case Reports; Research Support, Non-U.S. Gov't; Journal Article |
| Journal Info: | Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 2073-4425 |
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| DOI: | 10.3390/genes11121461 |
