✦ LIBER ✦

Wolfram (DIDMOAD) Syndrome and Leber Hereditary Optic Neuropathy (LHON) Are Associated with Distinct Mitochondrial DNA Haplotypes

✍ Scribed by Sabine Hofmann; Reimar Bezold; Michaela Jaksch; Bert Obermaier-Kusser; Sabine Mertens; Petra Kaufhold; Wolfgang Rabl; Wolfgang Hecker; Klaus-Dieter Gerbitz

Book ID: 115613614
Publisher: Elsevier Science
Year: 1997
Tongue: English
Weight: 167 KB
Volume: 39
Category: Article
ISSN: 0888-7543
DOI: 10.1006/geno.1996.4474

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A double mutation (G11778A and G12192A)

A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy

✍ M. Mimaki; A. Ikota; A. Sato; H. Komaki; J. Akanuma; I. Nonaka; Y. Goto 📂 Article 📅 2003 🏛 Nature Publishing Group 🌐 English ⚖ 229 KB

T14484C and T14502C in the mitochondrial

T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber’s hereditary optic neuropathy in a Chinese family

✍ Shirong Zhang; Lejin Wang; Yansheng Hao; Pengyun Wang; Ping Hao; Ke Yin; Qing K 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 737 KB