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Insulin gene mutations as a cause of permanent neonatal diabetes.
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Perspectives on the treatment of chronic phase and advanced phase CML and Philadelphia chromosome positive ALL(1).
To test or "NOD-2" test: what are the questions? The balanced viewpoint.
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Insulin gene mutations as a cause of permanent neonatal diabetes.
Insulin gene mutations as a cause of permanent neonatal diabetes. Proc Natl Acad Sci U S A. 2007 Sep 18; 104(38):15040-4.
View in:
PubMed
subject areas
Amino Acid Sequence
ATP-Binding Cassette Transporters
Diabetes Mellitus
Female
Genetic Linkage
Heterozygote
Humans
Infant
Infant, Newborn
Insulin
Male
Models, Biological
Molecular Sequence Data
Mutation, Missense
Pedigree
Potassium Channels
Potassium Channels, Inwardly Rectifying
Proinsulin
Protein Folding
Protein Precursors
Receptors, Drug
Sulfonylurea Receptors
authors with profiles
Susannah Spiess
Louis Philipson
Nancy Jean Cox
Graeme Bell
Siri Atma W. Greeley