Currarino syndrome: a comprehensive genetic review of a rare congenital disorder.
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| Title: | Currarino syndrome: a comprehensive genetic review of a rare congenital disorder. |
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| Authors: | Dworschak GC; Institute of Human Genetics, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127, Bonn, Germany. gabriel.dworschak@uni-bonn.de.; Institute of Anatomy and Cell Biology, Medical Faculty, University of Bonn, 53115, Bonn, Germany. gabriel.dworschak@uni-bonn.de.; Department of Pediatrics, University Hospital Bonn, 53127, Bonn, Germany. gabriel.dworschak@uni-bonn.de., Reutter HM; Institute of Human Genetics, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127, Bonn, Germany.; Department of Neonatology and Pediatric Intensive Care, University Hospital Bonn, 53127, Bonn, Germany., Ludwig M; Department of Clinical Chemistry and Clinical Pharmacology, University of Bonn, 53127, Bonn, Germany. |
| Source: | Orphanet journal of rare diseases [Orphanet J Rare Dis] 2021 Apr 09; Vol. 16 (1), pp. 167. Date of Electronic Publication: 2021 Apr 09. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't; Review |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| ISSN: | 1750-1172 |
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| DOI: | 10.1186/s13023-021-01799-0 |
