A novel variant of slc4a1 for hereditary spherocytosis in a chinese family: a case report and systematic review

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• who: Jie Li from the in the Indian population [12]Although relevant studies on HS in the Chinese population have been published in the last , years, in some cases, it is difficult to make a definite diagnosis due to the variable genotypic and phenotypic features of HS and the lack of well-documented evidence for HS patients. Timely diagnosis and therapy will help decrease complications of biliary tract disease, such as biliary obstruction with pancreatitis, cholecystitis, and cholangitis, and contribute to improving patients` quality of life [21315]. Thus, accurate detection of known or new variant sites associated . . .
  

   

  

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