Limb-girdle muscular dystrophy: an immunohistochemical diagnostic approach

The limb-girdle muscle dystrophy (LGMD) represents a heterogeneous group of muscular diseases with dominant and recessive inheritance, individualized by gene mutation. A group of 56 patients, 32 males and 24 females, with suggestive LGMD diagnosis were submitted to clinical evaluation, serum muscle...

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Bibliographic Details
Main Authors: Comerlato,Enio Alberto, Scola,Rosana Hermínia, Werneck,Lineu César
Format: Digital revista
Language:English
Published: Academia Brasileira de Neurologia - ABNEURO 2005
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2005000200009
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