✦ LIBER ✦

Association of Deletion and Homoplasmic Point Mutation of the Mitochondrial DNA in an Ocular Myopathy

✍ Scribed by P. Reynier; D. Figarellabranger; G. Serratrice; B. Charvet; Y. Malthiery

Book ID: 115575148
Publisher: Elsevier Science
Year: 1994
Tongue: English
Weight: 369 KB
Volume: 202
Category: Article
ISSN: 0006-291X
DOI: 10.1006/bbrc.1994.2116

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A tandem duplication in the D–loop of hu

A tandem duplication in the D–loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies

✍ Brockington, Martin; Sweeney, Mary G.; Hammans, Simon R.; Morgan-Hughes, John A. 📂 Article 📅 1993 🏛 Nature Publishing Group 🌐 English ⚖ 534 KB

Identical Mitochondrial DNA Deletion in

Identical Mitochondrial DNA Deletion in a Woman with Ocular Myopathy and in Her Son with Pearson Syndrome

✍ Sara Shanske; Yingying Tang; Michio Hirano; Yutaka Nishigaki; Kurenai Tanji; Edu 📂 Article 📅 2002 🏛 American Society of Human Genetics 🌐 English ⚖ 173 KB

Oculopharyngeal somatic myopathy in a pa

Oculopharyngeal somatic myopathy in a patient with a novel large-scale 3399 bp deletion and a homoplasmic T5814C transition of the mitochondrial DNA

✍ Peterus Thajeb; Yi-Shing Ma; Chin-Yuan Tzen; Chih-Kuang Chuang; Tsu-Yen Wu; Shiu 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 201 KB

3.080 MITOCHONDRIAL D-LOOP HOMOPLASMIC T

3.080 MITOCHONDRIAL D-LOOP HOMOPLASMIC T16519C POINT MUTATION AND IDENTIFICATION OF NOVEL MARKERS ASSOCIATED WITH FRDA PATIENTS IN INDIAN POPULATION

✍ I.S. Mudila; M. Faruq; A.K. Srivastava; M. Mukerji 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 51 KB

Mitochondrial maculopathy: geographic at

Mitochondrial maculopathy: geographic atrophy of the macula in the MELAS associated A to G 3243 mitochondrial DNA point mutation

✍ Paul Latkany; Thomas A. Ciulla; Paul Cucchillo; Marc D. Malkoff 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 363 KB

Cosegregation of the mitochondrial DNA A

Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathy

✍ Y. Campos; A. García; A. López; S. Jiménez; J.C. Rubio; P. Del Hoyo; F. Bustos; 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 230 KB