Novel COL6A2 mutation in a case of limb girdle muscular dystrophy phenotype with autosomal recessive inheritance

Publisher: John Wiley & Sons Inc

E-ISSN: 2049-4173|4|5|189-191

ISSN: 2049-4173

Source: Neurology And Clinical Neuroscience (Electronic), Vol.4, Iss.5, 2016-09, pp. : 189-191

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content