[HTML] nih.gov

[HTML][HTML] Identification of FECH gene multiple variations in two Chinese patients with erythropoietic protoporphyria and a review

Z Long, Y Wang, C Yang, G Liu, Y Du… - Journal of Zhejiang …, 2016 - ncbi.nlm.nih.gov
Erythropoietic protoporphyria (EPP), an autosomal dominant disease, is caused by partial
deficiency of ferrochelatase (FECH), which catalyzes the terminal step of heme biosynthesis …
被引用次数：5 相关文章

Identification of FECH gene multiple variations in two Chinese patients with erythropoietic protoporphyria and a review.

ZB Long, YW Wang, C Yang, G Liu, YL Du… - Journal of Zhejiang …, 2016 - europepmc.org
Erythropoietic protoporphyria (EPP), an autosomal dominant disease, is caused by partial
deficiency of ferrochelatase (FECH), which catalyzes the terminal step of heme biosynthesis …

Identification of FECH gene multiple variations in two Chinese patients with erythropoietic protoporphyria and a review

ZB Long, YW Wang, C Yang, G Liu… - Journal of Zhejiang …, 2016 - pubmed.ncbi.nlm.nih.gov
Erythropoietic protoporphyria (EPP), an autosomal dominant disease, is caused by partial
deficiency of ferrochelatase (FECH), which catalyzes the terminal step of heme biosynthesis …

Identification of FECH gene multiple variations in two Chinese patients with erythropoietic protoporphyria and a review

L Zhang-biao, W Yong-wei, Y Chen… - Journal of Zhejiang …, 2016 - search.proquest.com
Erythropoietic protoporphyria (EPP), an autosomal dominant disease, is caused by partial
deficiency of ferrochelatase (FECH), which catalyzes the terminal step of heme biosynthesis …
[HTML] zju.edu.cn

[HTML][HTML] Identification of FECH gene multiple variations in two Chinese patients with erythropoietic protoporphyria and a review

Z Long, Y Wang, C Yang, G Liu, Y Du, G Nie, Y Chang… - jzus.zju.edu.cn
Erythropoietic protoporphyria (EPP), an autosomal dominant disease, is caused by partial
deficiency of ferrochelatase (FECH), which catalyzes the terminal step of heme biosynthesis …
[PDF] researchgate.net

[PDF][PDF] Identification of FECH gene multiple variations in two Chinese patients with erythropoietic protoporphyria and a review

Z LONG, Y WANG, C YANG, G LIU, Y DU, G NIE… - 2016 - researchgate.net
Erythropoietic protoporphyria (EPP), an autosomal dominant disease, is caused by partial
deficiency of ferrochelatase (FECH), which catalyzes the terminal step of heme biosynthesis …
[HTML] zju.edu.cn

[HTML][HTML] Identification of FECH gene multiple variations in two Chinese patients with erythropoietic protoporphyria and a review

Z Long, Y Wang, C Yang, G Liu, Y Du, G Nie, Y Chang… - jzus.zju.edu.cn
Erythropoietic protoporphyria (EPP), an autosomal dominant disease, is caused by partial
deficiency of ferrochelatase (FECH), which catalyzes the terminal step of heme biosynthesis …

Identification of FECH gene multiple variations in two Chinese patients with erythropoietic protoporphyria and a review

Z Long, Y Wang, C Yang, G Liu, Y Du, G Nie… - Journal of Zhejiang …, 2016 - infona.pl
Erythropoietic protoporphyria (EPP), an autosomal dominant disease, is caused by partial
deficiency of ferrochelatase (FECH), which catalyzes the terminal step of heme biosynthesis …
[HTML] zju.edu.cn

[HTML][HTML] Identification of FECH gene multiple variations in two Chinese patients with erythropoietic protoporphyria and a review

Z Long, Y Wang, C Yang, G Liu, Y Du, G Nie, Y Chang… - jzus.zju.edu.cn
Erythropoietic protoporphyria (EPP), an autosomal dominant disease, is caused by partial
deficiency of ferrochelatase (FECH), which catalyzes the terminal step of heme biosynthesis …
[PDF] researchgate.net

[PDF][PDF] Identification of FECH gene multiple variations in two Chinese patients with erythropoietic protoporphyria and a review

Z LONG, Y WANG, C YANG, G LIU, Y DU, G NIE… - 2016 - researchgate.net
Erythropoietic protoporphyria (EPP), an autosomal dominant disease, is caused by partial
deficiency of ferrochelatase (FECH), which catalyzes the terminal step of heme biosynthesis …