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Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.

Authors
Type
Published Article
Journal
Ear and Hearing
0196-0202
Publisher
Ovid Technologies (Wolters Kluwer) - Lippincott Williams & Wilkins
Publication Date
Volume
28
Issue
3
Pages
332–342
Identifiers
PMID: 17485982
Source
Medline

Abstract

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