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Institute of Medical Genetics,
Center for Pathobiochemistry and Genetics,
Institute of Medical Genetics, Center for Pathobiochemistry and Genetics
Franco Laccone has not added Biography.
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Dysmorphic syndrome of hereditary neuralgic amyotrophy associated with a SEPT9 gene mutation--a family study.
Clinical genetics Sep, 2008 | Pubmed ID: 18492087
Desbuquois dysplasia type I and fetal hydrops due to novel mutations in the CANT1 gene.
European journal of human genetics : EJHG Nov, 2011 | Pubmed ID: 21654728
Familial, long-term pollakisuria as initial manifestation of HSP4 due to the SPAST variant c.683-2A>C.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia Jun, 2019 | Pubmed ID: 30962061
Medical University of Vienna (MUV)
Hannes Steinkellner1,
Alexander V. Beribisky1,
Philip Mausberg1,
John Christodoulou2,
Barbara Scheiber-Mojdehkar3,
Anna Huber1,
Victoria Sarne1,
Franco Laccone1
1Institute of Medical Genetics, Center for Pathobiochemistry and Genetics, Medical University of Vienna (MUV),
2Murdoch Children's Research Institute and Department of Paediatrics, University of Melbourne, Discipline of Child & Adolescent Health, Sydney Medical School,
3Department of Medical Chemistry and Pathobiochemistry, Medical University of Vienna
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