A Novel Mutation of Glutamate Dehydrogenase (H262Y) in an Infant with Hyperinsulinemic Hypoglycemia and Hyperammonemia

S. Halldorsdottir,; W.K. Chung,; J.F. Nicholson,; K. Das,; R.L. Leibel,

doi:10.1515/IJDHD.2000.1.4.235

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A Novel Mutation of Glutamate Dehydrogenase (H262Y) in an Infant with Hyperinsulinemic Hypoglycemia and Hyperammonemia

S. Halldorsdottir, , W.K. Chung, , J.F. Nicholson, , K. Das, und R.L. Leibel,

Veröffentlicht/Copyright: 1. Oktober 2000

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Aus der Zeitschrift International Journal on Disability and Human Development Band 1 Heft 4

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Halldorsdottir,, S., Chung,, W.K., Nicholson,, J.F., Das,, K. and Leibel,, R.L.. "A Novel Mutation of Glutamate Dehydrogenase (H262Y) in an Infant with Hyperinsulinemic Hypoglycemia and Hyperammonemia" International Journal on Disability and Human Development, vol. 1, no. 4, 2000, pp. 235-242. https://doi.org/10.1515/IJDHD.2000.1.4.235

Halldorsdottir,, S., Chung,, W., Nicholson,, J., Das,, K. & Leibel,, R. (2000). A Novel Mutation of Glutamate Dehydrogenase (H262Y) in an Infant with Hyperinsulinemic Hypoglycemia and Hyperammonemia. International Journal on Disability and Human Development, 1(4), 235-242. https://doi.org/10.1515/IJDHD.2000.1.4.235

Halldorsdottir,, S., Chung,, W., Nicholson,, J., Das,, K. and Leibel,, R. (2000) A Novel Mutation of Glutamate Dehydrogenase (H262Y) in an Infant with Hyperinsulinemic Hypoglycemia and Hyperammonemia. International Journal on Disability and Human Development, Vol. 1 (Issue 4), pp. 235-242. https://doi.org/10.1515/IJDHD.2000.1.4.235

Halldorsdottir,, S., Chung,, W.K., Nicholson,, J.F., Das,, K. and Leibel,, R.L.. "A Novel Mutation of Glutamate Dehydrogenase (H262Y) in an Infant with Hyperinsulinemic Hypoglycemia and Hyperammonemia" International Journal on Disability and Human Development 1, no. 4 (2000): 235-242. https://doi.org/10.1515/IJDHD.2000.1.4.235

Halldorsdottir, S, Chung, W, Nicholson, J, Das, K, Leibel, R. A Novel Mutation of Glutamate Dehydrogenase (H262Y) in an Infant with Hyperinsulinemic Hypoglycemia and Hyperammonemia. International Journal on Disability and Human Development. 2000;1(4): 235-242. https://doi.org/10.1515/IJDHD.2000.1.4.235

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Published Online: 2000-10

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Artikel in diesem Heft

CONTENTS
Letter from the Editors
Molecular Bases of Pathological Growth
A History of Medical Genetics in France
Local Homologies of Menin with Tumor Suppressor Gene Products and Other Proteins
Genomic Organization of the Human GHRELIN Gene
A Novel Mutation of Glutamate Dehydrogenase (H262Y) in an Infant with Hyperinsulinemic Hypoglycemia and Hyperammonemia
Brain Hamartoma in an Infant with Bannayan-Riley-Ruvalcaba Syndrome: Patient Report and Review of the Literature
Neonatal Hypothyroxinemia Secondary to Dysfunctional TBG
BOOK REVIEWS. CALENDAR. AUTHOR INDEX. SUBJECT INDEX

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https://doi.org/10.1515/IJDHD.2000.1.4.235

Artikel in diesem Heft

CONTENTS
Letter from the Editors
Molecular Bases of Pathological Growth
A History of Medical Genetics in France
Local Homologies of Menin with Tumor Suppressor Gene Products and Other Proteins
Genomic Organization of the Human GHRELIN Gene
A Novel Mutation of Glutamate Dehydrogenase (H262Y) in an Infant with Hyperinsulinemic Hypoglycemia and Hyperammonemia
Brain Hamartoma in an Infant with Bannayan-Riley-Ruvalcaba Syndrome: Patient Report and Review of the Literature
Neonatal Hypothyroxinemia Secondary to Dysfunctional TBG
BOOK REVIEWS. CALENDAR. AUTHOR INDEX. SUBJECT INDEX