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Aspartylglucosaminuria among Palestinian Arabs

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Solid-phase minisequencing confirmed by FISH analysis in determination of gene copy number

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Human Genetics, 1995, Volume 96, Number 3, Pages 275-280

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Splicing defect of the glycoasparaginase gene in two Japanese siblings with apartylglucosamimiria

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Human Genetics, 1992, Volume 90, Numbers 1-2, Pages 179-180

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Linkage of aspartylglucosaminuria (AGU) to marker loci on the long arm of chromosome 4

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Human Genetics, 1990, Volume 85, Number 2, Pages 233-236

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Single base deletion in exon 7 of the glycosylasparaginase gene causes a mild form of aspartylglycosaminuria in a patient of Mauritian origin

H. Park, M. Rossiter, A. H. Fensom, B. Winchester and N. N. Aronson

Journal of Inherited Metabolic Disease, 1996, Volume 19, Number 1, Pages 76-83

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Aspartylglycosaminuria in an Italian family: Clinical and biochemical characteristics

J. Gehler, A. C. Sewell, Christa Becker, J. Spranger and J. Hartmann

Journal of Inherited Metabolic Disease, 1981, Volume 4, Number 1, Pages 229-230

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Coordination of PsAS1 and PsASPG expression controls timing of re-allocated N utilization in hypocotyls of pine seedlings

Rafael A. Cañas, Fernando de la Torre, Francisco M. Cánovas and Francisco R. Cantón

Planta, 2006, Volume 225, Number 5, Pages 1205-1219

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