Literature DB >> 23255290

Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1.

Rob Van Zwieten, Jerney J J M François, Karin Van Leeuwen, Annet C W Van Wesel, Robin Van Bruggen, Wouter W Van Solinge, Dirk Roos, Arthur J Verhoeven, Richard Van Wijk.   

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Year:  2012        PMID： 23255290     DOI： 10.1002/ajh.23363

Source DB:  PubMed          Journal:  Am J Hematol        ISSN： 0361-8609            Impact factor:   10.047


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  3 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.  Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone Disease.

Authors:  Andrea G Cogal; Jennifer Arroyo; Ronak Jagdeep Shah; Kalina J Reese; Brenna N Walton; Laura M Reynolds; Gabrielle N Kennedy; Barbara M Seide; Sarah R Senum; Michelle Baum; Stephen B Erickson; Sujatha Jagadeesh; Neveen A Soliman; David S Goldfarb; Lada Beara-Lasic; Vidar O Edvardsson; Runolfur Palsson; Dawn S Milliner; David J Sas; John C Lieske; Peter C Harris
Journal:  Kidney Int Rep       Date:  2021-09-08

3.  Study on Management of Blood Transfusion Therapy in Patients with Hereditary Spherocytosis.

Authors:  Shiyue Ma; Lingjian Tang; Chaoli Wu; Hui Tang; Xue Pu; Jinhong Niu
Journal:  Appl Bionics Biomech       Date:  2022-01-28       Impact factor: 1.781
  3 in total

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