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

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Autoria(s): Remenyik, E; Lanyon, GW; Horkay, I; Paragh, G; Wikonkal, N; Kosa, A; Moore, MR

Data(s)	01/01/1998
Identificador	http://espace.library.uq.edu.au/view/UQ:35073
Idioma(s)	eng
Palavras-Chave	#Dermatology #Molecular Defect
Tipo	Journal Article