A Third Locus Predisposing to Multiple Deletions of mtDNA in Autosomal Dominant Progressive External Ophthalmoplegia

Author:

Kaukonen Jyrki,Zeviani Massimo,Comi Giacomo Pietro,Piscaglia Maria-Grazia,Peltonen Leena,Suomalainen Anu

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference24 articles.

1. Autosomal recessive Wolfram syndrome associated with an 8.5-kb mtDNA single deletion;Barrientos;Am J Hum Genet,1996

2. A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome;Barrientos;J Clin Invest,1996

3. Faster sequential genetic linkage computations;Cottingham;Am J Hum Genet,1993

4. A comprehensive genetic map of the human genome based on 5,264 microsatellites;Dib;Nature,1996

5. Assignment of the human muscle adenine nucleotide translocator gene (ANT1) to 4q35 by fluorescence in situ hybridization;Fan;Cytogenet Cell Genet,1992

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