(Q44564067)

English

Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptor.

scientific article published in September 2003

Statements

Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptor. (English)
0 references
Paul S Thornton
Courtney MacMullen
Arupa Ganguly
Eduardo Ruchelli
Linda Steinkrauss
Ana Crane
Lydia Aguilar-Bryan
1 September 2003
2403-2410

Identifiers

 
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