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

Antzeko izenburuak

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