Results 211 to 215 of about 15,103 (215)

Autosomal recessive myopathy without inclusion bodies caused by GNE gene mutation.

2006
R.DEL BO, M. GUGLIERI, M. G. D'Angelo, S. GHEZZI, F.MAGRI, L. NAPOLI, A. PRELLE, A. C. Turconi, M. MOGGIO, N. BRESOLIN, G.P. COMI.   +10 more
openaire   +1 more source

689PTracing ancient gene flow from Persia to Japan through a shared haplotype in GNE myopathy

Neuromuscular Disorders
W. Yoshioka, K. Sonehara, M. Bakhshandeh, M. Ogawa, K. Eguchi, S. Hayashi, Y. Okada, H. Najmabadi, MR Akbari, S. Noguchi, I. Nishino   +10 more
openaire   +1 more source

[Sequence of Escherichia coli O138 O-antigen gene cluster and gne identification by bioinformatics].

, 2004
Qing Ke Kong, Jian Cheng, Guang Zhao, Lei Wang, Hong Jie Guo   +4 more
openalex  

Co-existence of GNE gene mutation in a case of genetically defined oculopharingeal dystrophy

2009
Banfi P, MAURI, MARCO, Azan G, Corbetta S, Bono GG   +4 more
openaire   +1 more source

Co-existence of GNE gene mutation in a case of genetically assessed oculopharingeal muscolar dystrophy

2009
Banfi P, MAURI, MARCO, Azan G, Corbetta S, BONO, GIORGIO GIOVANNI   +4 more
openaire   +1 more source