Bodur, E. D. Et Al. 2021. THE FIRST CASE OF AMYLOIDOSIS DUE TO HOMOZYGOUS P.V377I MUTATION IN A PATIENT WITH HYPERIMMUNOGLOBULIN D SYNDROME. PEDIATRIC NEPHROLOGY , vol.36, no.10 , 3448.

Bodur, E. D., GÖKCE, İ., Sozeri, B., Alavanda, C., Farmanli, O., Ata, P., ... KAYA, H.(2021). THE FIRST CASE OF AMYLOIDOSIS DUE TO HOMOZYGOUS P.V377I MUTATION IN A PATIENT WITH HYPERIMMUNOGLOBULIN D SYNDROME. PEDIATRIC NEPHROLOGY , vol.36, no.10, 3448.

Bodur, Ece Et Al. "THE FIRST CASE OF AMYLOIDOSIS DUE TO HOMOZYGOUS P.V377I MUTATION IN A PATIENT WITH HYPERIMMUNOGLOBULIN D SYNDROME," PEDIATRIC NEPHROLOGY , vol.36, no.10, 3448, 2021

Bodur, Ece D. Et Al. "THE FIRST CASE OF AMYLOIDOSIS DUE TO HOMOZYGOUS P.V377I MUTATION IN A PATIENT WITH HYPERIMMUNOGLOBULIN D SYNDROME." PEDIATRIC NEPHROLOGY , vol.36, no.10, pp.3448, 2021

Bodur, E. D. Et Al. (2021) . "THE FIRST CASE OF AMYLOIDOSIS DUE TO HOMOZYGOUS P.V377I MUTATION IN A PATIENT WITH HYPERIMMUNOGLOBULIN D SYNDROME." PEDIATRIC NEPHROLOGY , vol.36, no.10, p.3448.

@article{article, author={Ece Demirci Bodur Et Al. }, title={THE FIRST CASE OF AMYLOIDOSIS DUE TO HOMOZYGOUS P.V377I MUTATION IN A PATIENT WITH HYPERIMMUNOGLOBULIN D SYNDROME}, journal={PEDIATRIC NEPHROLOGY}, year=2021, pages={3448} }