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Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment

✍ Scribed by Jacobs, Howard T; Hutchin, Timothy P; Käppi, Timo; Gillies, Greta; Minkkinen, Kia; Walker, John; Thompson, Karen; Rovio, Anja T; Carella, Massimo; Melchionda, Salvatore


Book ID
110025655
Publisher
Nature Publishing Group
Year
2004
Tongue
English
Weight
124 KB
Volume
13
Category
Article
ISSN
1018-4813

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Mitochondrial DNA mutations in patients
✍ Schwartz, Faina; Baldwin, Clinton T.; Baima, Jader; Gavras, Haralambos 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 45 KB 👁 2 views

We determined the entire sequence of the mitochondrial genome in affected individuals from three families with idiopathic orthostatic hypotension. The disorder in two of these families was recently linked to chromosome arm 18q, while the third family remains unlinked. In all three families, orthosta