红细胞生成性原卟啉症：一种导致人类亚铁螯合酶基因外显子跳跃的新突变。 - Suppr | 超能文献

Erythropoietic protoporphyria: a new mutation responsible for exon skipping in the human ferrochelatase gene.

作者信息

Remenyik E, Lanyon G W, Horkay I, Paragh G, Wikonkál N, Kósa A, Moore M R

出版信息

J Invest Dermatol. 1998 Sep;111(3):540-1. doi: 10.1046/j.1523-1747.1998.00300.x.

DOI:10.1046/j.1523-1747.1998.00300.x

Abstract

摘要

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