Literature DB >> 26852520

A NOVEL ASPARTYLGLUCOSAMINURIA MUTATION IN A PATIENT WITH CO-EXISTENCE OF GAUCHER DISEASE.

E Kiykim, T Zubarioglu, O Gorukmez, S Gunes, M S Cansever, A C Aktuglu Zeybek.   

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Year:  2015        PMID： 26852520

Source DB:  PubMed          Journal:  Genet Couns        ISSN： 1015-8146


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  1 in total

1.  Three mutations of adult type 1 Gaucher disease found in a Chinese patient: A case report.

Authors:  Xiaoli Du; Qian Ding; Qi Chen; Pengxiang Guo; Qing Wang
Journal:  Medicine (Baltimore)       Date:  2018-11       Impact factor: 1.889
  1 in total

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