Havali, C. Et Al. 2020. Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.33, no.3 , 437-441.

Havali, C., Dorum, S., Akbas, Y., Gorukmez, O., & HIRFANOĞLU, T., (2020). Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.33, no.3, 437-441.

Havali, Cengiz Et Al. "Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.33, no.3, 437-441, 2020

Havali, Cengiz Et Al. "Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.33, no.3, pp.437-441, 2020

Havali, C. Et Al. (2020) . "Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.33, no.3, pp.437-441.

@article{article, author={Cengiz Havali Et Al. }, title={Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2020, pages={437-441} }