Creatine metabolism in patients with urea cycle disorders.

Ingoglia, Filippo; Chong, Jean-Leon; Pasquali, Marzia; Longo, Nicola

Ingoglia, Filippo; Chong, Jean-Leon; Pasquali, Marzia; Longo, Nicola.

Affiliation

Ingoglia F; Department of Pathology, University of Utah, Salt Lake City, UT 84108, USA.
Chong JL; ARUP Laboratories, 500 Chipeta Way, Salt Lake City, UT 84108, USA.
Pasquali M; Department of Pathology, University of Utah, Salt Lake City, UT 84108, USA.
Longo N; ARUP Laboratories, 500 Chipeta Way, Salt Lake City, UT 84108, USA.

Mol Genet Metab Rep ; 29: 100791, 2021 Dec.

Article in En | MEDLINE | ID: mdl-34471603

Key words

AGAT, arginine glycine amidinotransferase; ASL, argininosuccinate lyase; ASS, argininosuccinate synthase; Arginase deficiency; Arginine; CT1, creatine transporter 1; Creatine; Creatine deficiency; GAA, guanidinoacetate; GAMT, guanidino acetate methyltransferase; Guanidinoacetate; NOS, nitric oxide synthase; ORNT1, ornithine transporter 1; OTC, ornithine transcarbamylase; SLC6A8, solute carrier family 6 member 8 gene; UCD, urea cycle disorders; Urea cycle defect

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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Genet Metab Rep Year: 2021 Type: Article Affiliation country: United States

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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Genet Metab Rep Year: 2021 Type: Article Affiliation country: United States