𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutation at nucleotide position 3243 of the mitochondrial DNA as a cause of IDDM – a meta-analysis

✍ Scribed by M. Odawara; K. Yamashita


Publisher
Springer
Year
1997
Tongue
English
Weight
89 KB
Volume
40
Category
Article
ISSN
0012-186X

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Dystonia as a presenting feature of the
✍ Lewis Sudarsky; George M. Plotkin; Eric L. Logigian; Donald R. Johns 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 56 KB 👁 2 views

A variety of neurologic phenotypes have been described in patients with mitochondrial disorders. We report a 32-year-old man in whom dystonia was the salient and presenting feature of a mitochondrial DNA mutation. He presented at age 23 with writer's cramp and progressed over 5 years to exhibit dyst

Quantitative allele-specific PCR: Demons
✍ Vincent W. S. Liu; Chunfang Zhang; Anthony W. Linnane; Phillip Nagley 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 167 KB 👁 2 views

We have developed an improved allele-specific polymerase chain reaction (AS-PCR) procedure that can selectively amplify mutant DNA sequences (which differ from the normal sequences by a single base pair) in the presence of large excess of normal sequences. We applied this procedure to quantification

Maternally inherited cardiomyopathy: A n
✍ Gabriella Silvestri; Enrico Bertini; Serenella Servidei; Michele Rana; Elisabett 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 296 KB 👁 2 views

The A to G transition at nt.3243 of the tRNA Leu(UUR) gene of mtDNA, commonly associated with MELAS, was detected in several members of a family affected by a maternally inherited form of hypertrophic cardiomyopathy. These findings suggest adding cardiomyopathy in the list of phenotypes associated w