Camtosun, E. Et Al. 2015. A Deep Intronic HADH Splicing Mutation (c.636+471G > T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.7, no.2 , 144-147.

Camtosun, E., Flanagan, S. E., Ellard, S., ŞIKLAR, Z., Hussain, K., Kocaay, P., ... BERBEROĞLU, M.(2015). A Deep Intronic HADH Splicing Mutation (c.636+471G > T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.7, no.2, 144-147.

Camtosun, Emine Et Al. "A Deep Intronic HADH Splicing Mutation (c.636+471G > T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course," JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.7, no.2, 144-147, 2015

Camtosun, Emine Et Al. "A Deep Intronic HADH Splicing Mutation (c.636+471G > T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course." JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.7, no.2, pp.144-147, 2015

Camtosun, E. Et Al. (2015) . "A Deep Intronic HADH Splicing Mutation (c.636+471G > T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course." JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.7, no.2, pp.144-147.

@article{article, author={Emine Camtosun Et Al. }, title={A Deep Intronic HADH Splicing Mutation (c.636+471G > T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course}, journal={JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY}, year=2015, pages={144-147} }