遗传性红细胞多核伴酸化血清试验阳性（HEMPAS）中的红细胞异常 - Suppr

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超能文献

Red-cell abnormalities in HEMPAS (hereditary erythroblastic multinuclearity with a positive acidified-serum test).

作者信息

Crookston J H, Crookston M C, Rosse W F

出版信息

Br J Haematol. 1972 Sep;23:Suppl:83-91. doi: 10.1111/j.1365-2141.1972.tb03507.x.

DOI:10.1111/j.1365-2141.1972.tb03507.x

PMID:4567203

Abstract

摘要

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Red-cell abnormalities in HEMPAS (hereditary erythroblastic multinuclearity with a positive acidified-serum test).遗传性红细胞多核伴酸化血清试验阳性（HEMPAS）中的红细胞异常

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Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.影响分泌性COPII包被组分SEC23B的突变会导致II型先天性红细胞生成异常性贫血。

Nat Genet. 2009 Aug;41(8):936-40. doi: 10.1038/ng.405. Epub 2009 Jun 28.

Congenital dyserythropoietic anaemia type II (HEMPAS): a family study.II型先天性红细胞生成异常性贫血（HEMPAS）：一项家族研究。

J Clin Pathol. 1980 Dec;33(12):1197-201. doi: 10.1136/jcp.33.12.1197.

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Congenital dyserythropoietic anemia, type II (Hempas). First five reported cases in Italy.先天性红细胞生成异常性贫血II型（遗传性多核幼红细胞增多症）。意大利首次报告的5例病例。

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[Congenital dyserythropoietic anemias].

Blut. 1975 Nov;31(5):261-70. doi: 10.1007/BF01634142.

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Blut. 1977 Dec;35(6):437-46. doi: 10.1007/BF00996690.

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