KARA, B. Et Al. 2021. A Novel Mutation of HINT1 Gene in an Adolescent Female with Axonal Neuropathy and Neuromyotonia. JOURNAL OF PEDIATRIC NEUROLOGY , vol.19, no.3 , 180-182.

KARA, B., Gul, S., SAKARYA GÜNEŞ, A., MÜLAYİM, S., & Yesil, G., (2021). A Novel Mutation of HINT1 Gene in an Adolescent Female with Axonal Neuropathy and Neuromyotonia. JOURNAL OF PEDIATRIC NEUROLOGY , vol.19, no.3, 180-182.

KARA, BÜLENT Et Al. "A Novel Mutation of HINT1 Gene in an Adolescent Female with Axonal Neuropathy and Neuromyotonia," JOURNAL OF PEDIATRIC NEUROLOGY , vol.19, no.3, 180-182, 2021

KARA, BÜLENT Et Al. "A Novel Mutation of HINT1 Gene in an Adolescent Female with Axonal Neuropathy and Neuromyotonia." JOURNAL OF PEDIATRIC NEUROLOGY , vol.19, no.3, pp.180-182, 2021

KARA, B. Et Al. (2021) . "A Novel Mutation of HINT1 Gene in an Adolescent Female with Axonal Neuropathy and Neuromyotonia." JOURNAL OF PEDIATRIC NEUROLOGY , vol.19, no.3, pp.180-182.

@article{article, author={BÜLENT KARA Et Al. }, title={A Novel Mutation of HINT1 Gene in an Adolescent Female with Axonal Neuropathy and Neuromyotonia}, journal={JOURNAL OF PEDIATRIC NEUROLOGY}, year=2021, pages={180-182} }