Open AccessOsteogenesis Imperfecta or Fanconi-Bickel Syndrome? (Report of a Very Rare Disease Due to New Mutation on GLUT2 Gene)
Author(s) -
Y. Shafaghati,
Peymaneh Sarkheil,
Taghi Baghdadi,
Fatemeh Hadipour,
Zahra Hadipour,
Mehrdad Noruzinia
Publication year - 2016
Publication title -
sarem journal of reproductive medicine
Language(s) - English
Resource type - Journals
eISSN - 2476-3470
pISSN - 2251-8215
DOI - 10.29252/sjrm.1.2.73
Subject(s) - glut2 , osteogenesis imperfecta , mutation , gene , genetics , fanconi syndrome , medicine , biology , anatomy , gene expression , kidney
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