A novel mutation in the porphobilinogen deaminase gene in an extended Chinese family with acute intermittent porphyria-Reference-Cited by-同舟云学术

A novel mutation in the porphobilinogen deaminase gene in an extended Chinese family with acute intermittent porphyria

Published:2015-07 Issue:2 Volume:565 Page:288-290
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Yang Jing,Wang Honglian,Yin Kunlun,Hua Baolai,Zhu Tienan,Zhao Yongqiang,Guo Shubin,Yu Xuezhong,Wu Wei,Zhou Zhou

Publisher

Elsevier BV

Subject

Genetics,General Medicine

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3. Three single nucleotide polymorphisms of porphobilinogen deaminase gene related to a Chinese patient with acute intermittent porphyria;Cao;Zhonghua Yi Xue Za Zhi,2008

4. One case of acute intermittent porphyria;Chen;Chin. J. Emerg. Med.,2011

5. Biochemical and hematological analysis in acute intermittent porphyria (AIP): a case report;Dos;An. Acad. Bras. Cienc.,2013

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