Large scale genotype–phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy-Reference-Cited by-同舟云学术

Large scale genotype–phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy

Published:2013-09-11 Issue:11 Volume:136 Page:3408-3417
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Ricci Giulia,Scionti Isabella,Sera Francesco,Govi Monica,D’Amico Roberto,Frambolli Ilaria,Mele Fabiano,Filosto Massimiliano,Vercelli Liliana,Ruggiero Lucia,Berardinelli Angela,Angelini Corrado,Antonini Giovanni,Bucci Elisabetta,Cao Michelangelo,Daolio Jessica,Di Muzio Antonio,Di Leo Rita,Galluzzi Giuliana,Iannaccone Elisabetta,Maggi Lorenzo,Maruotti Valerio,Moggio Maurizio,Mongini Tiziana,Morandi Lucia,Nikolic Ana,Pastorello Ebe,Ricci Enzo,Rodolico Carmelo,Santoro Lucio,Servida Maura,Siciliano Gabriele,Tomelleri Giuliano,Tupler Rossella

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/136/11/3408/13795480/awt226.pdf

Reference33 articles.

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2. Very low penetrance in 85 Japanese families with facioscapulohumeral muscular dystrophy 1A;Goto;J Med Genet,2004

3. Genetics of facioscapulohumeral muscular dystrophy: new mutations in sporadic cases;Griggs;Neurology,1993

4. Derivation and validation of QRISK, a new cardiovascular disease risk score for the United Kingdom: prospective open cohort study;Hippisley-Cox;BMJ,2007

5. Nonparametric estimation from incomplete observations;Kaplan;J Am Stat Assoc,1958

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