A case of a Japanese patient with neonatal diabetes mellitus caused by a novel mutation in the ABCC8 gene and successfully controlled with oral glibenclamide

مواد مشابهة

• A case of transient neonatal diabetes due to a novel mutation in ABCC8
  بواسطة: Takagi, Masaki, وآخرون
  منشور في: (2016)
• A case of spondyloepiphyseal dysplasia tarda caused by a novel intragenic deletion of TRAPPC2
  بواسطة: Takagi, Masaki, وآخرون
  منشور في: (2015)
• A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1
  بواسطة: Higuchi, Shinji, وآخرون
  منشور في: (2016)
• A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3
  بواسطة: Nagahara, Keiko, وآخرون
  منشور في: (2016)
• A familial case of spondyloepiphyseal dysplasia tarda caused by a novel splice site mutation in TRAPPC2
  بواسطة: Fukuma, Mami, وآخرون
  منشور في: (2018)