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Massive parallel sequencing as a new diagnostic approach for phenylketonuria and tetrahydrobiopterin-deficiency in Thailand.

Pongsathorn ChaiyasapChupong IttiwutChalurmpon SrichomthongApiruk SangsinKanya SuphapeetipornVorasuk Shotelersuk
Published in: BMC medical genetics (2017)
This study identified three novel mutations in either the PAH or PTS gene and supported the use of NGS as an alternative molecular genetic approach for definite diagnosis of hyperphenylalaninemia, thus leading to proper management of these patients in Thailand.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • genome wide
  • newly diagnosed
  • chronic kidney disease
  • copy number
  • prognostic factors
  • peritoneal dialysis
  • single cell
  • single molecule