Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred

L.K. Sprunger,; Μ.Η. Meisler,; C.A. Stratakis,

doi:10.1515/IJDHD.2000.1.3.165

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Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred

L.K. Sprunger, , Μ.Η. Meisler, and C.A. Stratakis,

Published/Copyright: July 1, 2000

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From the journal International Journal on Disability and Human Development Volume 1 Issue 3

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Sprunger,, L.K., Meisler,, Μ.Η. and Stratakis,, C.A.. "Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred" International Journal on Disability and Human Development, vol. 1, no. 3, pp. 165-170. https://doi.org/10.1515/IJDHD.2000.1.3.165

Sprunger,, L., Meisler,, Μ. & Stratakis,, C. (). Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred. International Journal on Disability and Human Development, 1(3), 165-170. https://doi.org/10.1515/IJDHD.2000.1.3.165

Sprunger,, L., Meisler,, Μ. and Stratakis,, C. () Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred. International Journal on Disability and Human Development, Vol. 1 (Issue 3), pp. 165-170. https://doi.org/10.1515/IJDHD.2000.1.3.165

Sprunger,, L.K., Meisler,, Μ.Η. and Stratakis,, C.A.. "Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred" International Journal on Disability and Human Development 1, no. 3 (): 165-170. https://doi.org/10.1515/IJDHD.2000.1.3.165

Sprunger, L, Meisler, Μ, Stratakis, C. Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred. International Journal on Disability and Human Development. ;1(3): 165-170. https://doi.org/10.1515/IJDHD.2000.1.3.165

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Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred
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https://doi.org/10.1515/IJDHD.2000.1.3.165

Articles in the same Issue

CONTENTS
Letter from the Editors
Prader-Willi and Angelman Syndromes: Diagnostic Approach
Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene
Novel Mutation (Arg836ter) of the Sulfonylurea Receptor-1 (SUR1) Gene in Congenital Hyperinsulinism
De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair
Bromocriptine Resistant Prolactinomas and Non-Functioning Pituitary Tumors: Somatic Mutational Analyses of the Dopamine Type 2 Receptor and the MEN1 Gene
Genetic Studies in Familial Aldosteronism Not Suppressible by Dexamethasone
Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred
BOOK REVIEWS. CALENDAR