Familial hyperinsulinism maps to chromosome 11p14–15.1, 30 cM centromeric to the insulin gene
Glaser, B. ; Chiu, K.C. ; Anker, R. ; Nestorowicz, A. ; Landau, H. ; Ben-Bassat, H. ; Shlomai, Z. ; Kaiser, N. ; Thornton, P.S. ; Stanley, C.A. ; Spielman, R.S. ; Gogolin-Ewens, K. ; Cerasi, E. ; Baker, L. ; Rice, J. ; Donis-Keller, H. ; Permutt, M.A.
[s.l.] : Nature Publishing Group
Published 1994
[s.l.] : Nature Publishing Group
Published 1994
| ISSN: |
1546-1718
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|---|---|
| Source: |
Nature Archives 1869 - 2009
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| Topics: |
Biology
Medicine
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| Notes: |
[Auszug] Familial hyperinsulinism (HI) is the most common cause of persistent neonatal hyperinsulinaemic hypoglycemia. Linkage analysis in 15 families (12 Ashkenazi Jewish, 2 consanguineous Arab, 1 non–Jewish Caucasian) mapped HI to chromosome 11p14–15.1 (lod score = 9.5, θ=0 at D11S921). ...
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| Type of Medium: |
Electronic Resource
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| URL: |