P.5.8 Why is LGMD2G rare?

Mutations in telethonin gene cause a rare and relatively mild form of limb-girdle muscular dystrophy type 2G. Only few families were described presenting this disease, and they are mainly Brazilians. In Brazil, this form represents less than 5% of all LGMD. In other countries, only isolated sporadic...

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Veröffentlicht in:	Neuromuscular disorders : NMD 2013-10, Vol.23 (9), p.766-766
Hauptverfasser:	Almeida, C.F, Onofre-Oliveira, P.C.G, Zatz, M, Negrao, L, Vainzof, M
Format:	Artikel
Sprache:	eng
Schlagworte:	Neurology
Online-Zugang:	Volltext
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