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Health / Rare diseases / Guanidines / Pediatrics / Argininosuccinate lyase / Genes / Urea cycle disorder / Argininosuccinic aciduria / Argininosuccinic acid / Urea cycle / Biology / Metabolism


ARGININOSUCCINIC ACIDURIA (ASA) REFERENCES (ARGININOSUCCINASE DEFICIENCY; ARGININOSUCCINATE LYASE DEFICIENCY; ASL DEFICIENCY; ARGININOSUCCINIC ACID LYASE DEFICIENCY[removed].
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Document Date: 2007-06-25 16:35:48

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City

Maestri / New York / OMIM / /

Company

Sumlin AB / Linnebank / Ishak KG. / Sperling LC / HP / /

Facility

Arch Dis Child / /

MedicalCondition

Inherited Disease / metabolic diseases / Acid Lyase Deficiency / neonatal argininosuccinate lyase deficiency / urea cycle disorders / ARGININOSUCCINASE DEFICIENCY / Inborn Errors of Metabolism / deficiency / argininosuccinate synthetase deficiency / MS / Systematic Disease / urea cycle enzyme disorders / disorders / ASL DEFICIENCY / ARGININOSUCCINATE LYASE DEFICIENCY / ARGININOSUCCINIC ACID LYASE DEFICIENCY / Other Urea Cycle Disorders / /

Organization

Colombo JP / /

Person

Scott Med / /

Position

Workman / /

Product

enflurane / /

ProvinceOrState

Nebraska / New York / /

Technology

spectroscopy / ASL / /

URL

www.geneclinics.org / /

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