Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (vol 90, pg 457, 2012)

Tuschl Karin; Clayton Peter T.; Gospe Sidney M. Jr.; Gulab Shamshad; Ibrahim Shahnaz; Singhi Pratibha; Aulakh Roosy; Ribeiro Reinaldo T.; Barsottini Orlando G.; Zaki Maha S.; Del Rosario Maria Luz; Dyack Sarah; Price Victoria; Rideout Andrea; Gordon Kevin; Wevers Ron A.; Chong W. K. Kling; Mills Philippa B.

首页> 外文期刊>The American Journal of Human Genetics >Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (vol 90, pg 457, 2012)

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Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (vol 90, pg 457, 2012)

机译：人体中的锰转运蛋白SLC30A10突变引起的肝硬化，肌张力障碍，红细胞增多症和高锰血症综合征（第90卷，第457页，2012年）

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来源
《The American Journal of Human Genetics》 |2016年第2期|共1页
作者
Tuschl Karin; Clayton Peter T.; Gospe Sidney M. Jr.; Gulab Shamshad; Ibrahim Shahnaz; Singhi Pratibha; Aulakh Roosy; Ribeiro Reinaldo T.; Barsottini Orlando G.; Zaki Maha S.; Del Rosario Maria Luz; Dyack Sarah; Price Victoria; Rideout Andrea; Gordon Kevin; Wevers Ron A.; Chong W. K. Kling; Mills Philippa B.;
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正文语种 eng
中图分类医学遗传学;
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1. Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (vol 90, pg 457, 2012) [J] . Tuschl Karin, Clayton Peter T., Gospe Sidney M. Jr., The American Journal of Human Genetics . 2016,第2期

机译：人体中的锰转运蛋白SLC30A10突变引起的肝硬化，肌张力障碍，红细胞增多症和高锰血症综合征（第90卷，第457页，2012年）
2. Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man [J] . TuschlK., ClaytonP.T., GospeJr.S.M., The American Journal of Human Genetics . 2012,第3期

机译：人体中的锰转运蛋白SLC30A10突变引起的肝硬化，肌张力障碍，红细胞增多症和高锰血症的综合征
3. A case of dystonia with polycythemia and hypermanganesemia caused by SLC30A10 mutation: a treatable inborn error of manganese metabolism [J] . Azita Tavasoli, Khadije Arjmandi Rafsanjani, Saba Hemmati, BMC Pediatrics . 2019,第1期

机译：由SLC30A10突变引起的多胆血症和HyperManganeSemia的肌肌瘤的病例：锰代谢的可治疗原问题
4. Syndrome of Hepatic Cirrhosis Dystonia Polycythemia and Hypermanganesemia Caused by Mutations in SLC30A10 a Manganese Transporter in Man [O] . Karin Tuschl, Peter T. Clayton, Sidney M. Gospe Jr., 2016

机译：锰转运蛋白SLC30A10突变引起的肝硬化肌张力障碍红细胞增多症和高锰血症综合征
5. Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man [O] . Tuschl Karin, Clayton Peter T., Gospe Sidney M., 2012

机译：锰转运蛋白SLC30A10突变引起的肝硬化，肌张力障碍，红细胞增多症和高锰血症综合征

Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (vol 90, pg 457, 2012)

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