The First Korean Case of HDR Syndrome Confirmed by Clinical and Molecular Investigation

Lignende værker

• The First Korean case of combined oxidative phosphorylation deficiency-17 diagnosed by clinical and molecular investigation
  af: Kim, Young A, et al.
  Udgivet: (2017)
• The First Korean Case of Mucopolysaccharidosis IIIC (Sanfilippo Syndrome Type C) Confirmed by Biochemical and Molecular Investigation
  af: Huh, Hee Jae, et al.
  Udgivet: (2013)
• A Korean boy with atypical X-linked adrenoleukodystrophy confirmed by an unpublished mutation of ABCD1
  af: Jwa, Hye Jeong, et al.
  Udgivet: (2014)
• Clinical, endocrinological, and molecular features of four Korean cases of cytochrome P450 oxidoreductase deficiency
  af: Lee, Yena, et al.
  Udgivet: (2020)
• A Korean boy with atypical X-linked adrenoleukodystrophy confirmed by an unpublished mutation of
  af: Hye Jeong Jwa, et al.
  Udgivet: (2014-09-01)