TEBER, S. Et Al. 2008. Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 gene. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.12, no.2 , 133-136.

TEBER, S., Sezer, T., Kafalt, M., Manzini, M. C., Yuksel, B. K., Tekin, M., ... FİTOZ, Ö. S.(2008). Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 gene. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.12, no.2, 133-136.

TEBER, SERAP Et Al. "Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 gene," EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.12, no.2, 133-136, 2008

TEBER, SERAP Et Al. "Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 gene." EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.12, no.2, pp.133-136, 2008

TEBER, S. Et Al. (2008) . "Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 gene." EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.12, no.2, pp.133-136.

@article{article, author={SERAP TEBER Et Al. }, title={Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 gene}, journal={EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY}, year=2008, pages={133-136} }