Cinar, M. Et Al. 2022. Spectrum of PAH gene mutations and genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Turkey. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.35, no.5 , 639-647.

Cinar, M., Yildirim, G. K., KOCAGİL, S., & ÇİLİNGİR, O., (2022). Spectrum of PAH gene mutations and genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Turkey. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.35, no.5, 639-647.

Cinar, MÜGE Et Al. "Spectrum of PAH gene mutations and genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Turkey," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.35, no.5, 639-647, 2022

Cinar, MÜGE Et Al. "Spectrum of PAH gene mutations and genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Turkey." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.35, no.5, pp.639-647, 2022

Cinar, M. Et Al. (2022) . "Spectrum of PAH gene mutations and genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Turkey." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.35, no.5, pp.639-647.

@article{article, author={MÜGE ÇINAR Et Al. }, title={Spectrum of PAH gene mutations and genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Turkey}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2022, pages={639-647} }