B. TÜYSÜZ Et Al. , "Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population," NEUROGENETICS , vol.9, no.2, pp.119-125, 2008
TÜYSÜZ, B. Et Al. 2008. Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population. NEUROGENETICS , vol.9, no.2 , 119-125.
TÜYSÜZ, B., BAYRAKLI, F., DiLuna, M. L., Bilguvar, K., BAYRİ, Y., YALÇINKAYA, C., ... Bursalı, A.(2008). Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population. NEUROGENETICS , vol.9, no.2, 119-125.
TÜYSÜZ, BEYHAN Et Al. "Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population," NEUROGENETICS , vol.9, no.2, 119-125, 2008
TÜYSÜZ, BEYHAN Et Al. "Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population." NEUROGENETICS , vol.9, no.2, pp.119-125, 2008
TÜYSÜZ, B. Et Al. (2008) . "Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population." NEUROGENETICS , vol.9, no.2, pp.119-125.
@article{article, author={BEYHAN TÜYSÜZ Et Al. }, title={Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population}, journal={NEUROGENETICS}, year=2008, pages={119-125} }