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Biochemical Genetics|June 1, 1985
Human lactase and the molecular basis of lactase persistenceJ Potter, M W Ho, H Bolton, et al.
Biochimica Et Biophysica Acta|March 20, 1992
Ageing of the human corneal stroma: structural and biochemical changesN S Malik, S J Moss, N Ahmed, et al.
Human Mutation|August 14, 1999
Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinismB Glaser, J Furth, C A Stanley, et al.
Diabetes, Obesity & Metabolism|August 30, 2012
Glucose metabolism: key endogenous regulator of β-cell replication and survivalD Dadon, S Tornovsky-Babaey, J Furth-Lavi, et al.
Nature Genetics|September 6, 2000
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C geneM Bitner-Glindzicz, K J Lindley, P Rutland, et al.
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