article · 2019
A neonate with hyperornithinemia-hyperammonemiahomocitrullinuria syndrome from a consanguineous Pakistani family
Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome is a rare autosomal recessive urea cycle disorder. HHH is caused by a deficiency of the mit...
0 citationsDOI: https://doi.org/10.5734/jgm.2019.16.2.85Open accessPDF reported by metadataFull text reported by metadata