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Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: Evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain

✍ Scribed by Tomoko Makishima; Anne C. Madeo; Carmen C. Brewer; Christopher K. Zalewski; John A. Butman; Vandana Sachdev; Andrew E. Arai; Brenda M. Holbrook; Douglas R. Rosing; Andrew J. Griffith


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
317 KB
Volume
143A
Category
Article
ISSN
1552-4825

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