Dystrophin characterization in BMD patients: correlation of abnormal protein with clinical phenotype-Reference-Cited by-同舟云学术

Dystrophin characterization in BMD patients: correlation of abnormal protein with clinical phenotype

Published:1995-10 Issue:2 Volume:132 Page:146-155
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Morandi Lucia,Mora Marina,Confalonieri Valeria,Barresi Rita,Di Blasi Claudia,Brugnoni Raffaella,Bernasconi Pia,Mantegazza Renato,Dworzak Federica,Antozzi Carlo,Balestrini Maria Rosa,Jarre Laura,Pini Antonella,Merlini Luciano,Piccolo Giovanni,Mazzanti Adriana,Daniel Sergio,Blàsevich Flavia,Cornelio Ferdinando

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

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4. Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific of dystrophin;Bulman;Am. J. Hum. Genet.,1991

5. The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalities;Bushby;J. Neurol.,1993

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