Suchergebnisse - "Haliloglu, Goknur"

PubPharm (6)

1

Selenoprotein N-related myopathy : a retrospective natural history study to guide clinical trials

enthalten in: Annals of clinical and translational neurology | 2020

von Silwal, A. | Sarkozy, A. | Scoto, M. | +16

2

Genetic Landscape of Congenital Myasthenic Syndromes From Turkey : Novel Mutations and Clinical Insights

enthalten in: Journal of child neurology | 2017

von Yiş, U. | Becker, K. | Kurul, S. | +13

3

SPEG interacts with myotubularin, and its deficiency causes centronuclear myopathy with dilated cardiomyopathy

enthalten in: American journal of human genetics | 2014

von Agrawal, P. | Pierson, C. | Joshi, M. | +13

4

Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy

enthalten in: American journal of human genetics | 2013

von Ravenscroft, G. | Miyatake, S. | Lehtokari, V. | +52

5

Calpain-3 mutations in Turkey

enthalten in: European journal of pediatrics | 2006

von Balci, B. | Aurino, S. | Haliloglu, G. | +9

6

A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycan

enthalten in: Neuromuscular disorders : NMD | 2003

von Dinçer, P. | Balci, B. | Yuva, Y. | +13

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