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Voice in Friedreich Ataxia

Published:2017-03 Issue:2 Volume:31 Page:243.e9-243.e19
ISSN:0892-1997
Container-title:Journal of Voice
language:en
Short-container-title:Journal of Voice

Author:

Vogel Adam P.,Wardrop Mayumi I.,Folker Joanne E.,Synofzik Matthis,Corben Louise A.,Delatycki Martin B.,Awan Shaheen N.

Publisher

Elsevier BV

Subject

LPN and LVN,Speech and Hearing,Otorhinolaryngology

Reference64 articles.

1. Clinical and genetic abnormalities in patients with Friedreich's ataxia;Durr;N Engl J Med,1996

2. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion;Campuzano;Science,1996

3. The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia;Filla;Am J Hum Genet,1996

4. Diagnosis and treatment of Friedreich ataxia: a European perspective;Schulz;Nat Rev Neurol,2009

5. Friedreich ataxia: an overview;Delatycki;J Med Genet,2000

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