Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease
作者： D Roos , M de Boer , F Kuribayashi , C Meischl , RS Weening
DOI: 10.1182/BLOOD.V87.5.1663.1663
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摘要:
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sci-hub.se 参考文章(1)
LC Tanugi-Cholley, JP Issartel, J Lunardi, F Freycon, F Morel, PV Vignais, A mutation located at the 5' splice junction sequence of intron 3 in the p67phox gene causes the lack of p67phox mRNA in a patient with chronic granulomatous disease. Blood. ,vol. 85, pp. 242- 249 ,(1995) , 10.1182/BLOOD.V85.1.242.BLOODJOURNAL851242