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A Patient with Type 2 Diabetes Mellitus Associated with Mutations in Calcium Sensing Receptor Gene and Mitochondrial DNA

โœ Scribed by Eizo Ohkubo; Kaoru Aida; Jing Chen; Jun-Ichi Hayashi; Kotoyo Isobe; Masato Tawata; Toshimasa Onaya


Book ID
115586947
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
161 KB
Volume
278
Category
Article
ISSN
0006-291X

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Heteroplasmy levels of a mitochondrial g
โœ Leen M. 't Hart; Janna J. Jansen; Herman H.P.J. Lemkes; Peter de Knijff; J. Anto ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 492 KB ๐Ÿ‘ 2 views

We showed previously that a mutation in the mitochondria1 tRNAL"(UUR' gene at position 3243 associates with maternally inherited diabetes and deafness (MIDD). This mutation shows heteroplasmy in DNA from peripheral blood and other tissues. To examine whether heteroplasmy levels in peripheral blood D