Author:
Bode Heiko,Bourquin Florence,Suriyanarayanan Saranya,Wei Yu,Alecu Irina,Othman Alaa,Von Eckardstein Arnold,Hornemann Thorsten
Funder
the 7th Framework Program of the European Commission
Swiss National Foundation SNF
Hurka Foundation, the Novartis Foundation and the Rare Disease Initiative Zurich (‘radiz’, Clinical Research Priority Program for Rare Diseases, University of Zurich)
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Reference66 articles.
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5. Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I);Houlden;Brain,2006
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