Literature DB >> 28280995

A de novo ankyrin mutation (ANK1 Q109X) causing severe hereditary spherocytosis from preterm neonatal period.

Sha Liu1, Hua Jiang1, Lv-Yin Huang2, Dong-Zhi Li3.   

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Year:  2017        PMID： 28280995     DOI： 10.1007/s00277-017-2966-1

Source DB:  PubMed          Journal:  Ann Hematol        ISSN： 0939-5555            Impact factor:   3.673


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  2 in total

Review 1.  Old and new insights into the diagnosis of hereditary spherocytosis.

Authors:  Olga Ciepiela
Journal:  Ann Transl Med       Date:  2018-09

2.  Severe hyperbilirubinemia in a neonate with hereditary spherocytosis due to a de novo ankyrin mutation: A case report.

Authors:  Jun-Fang Wang; Li Ma; Xiao-Hui Gong; Cheng Cai; Jing-Jing Sun
Journal:  World J Clin Cases       Date:  2021-07-06       Impact factor: 1.337
  2 in total

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