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A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family

✍ Scribed by Redouane Boulouiz; Yun Li; Hafid Soualhine; Omar Abidi; Abdelaziz Chafik; Gudrun Nürnberg; Christian Becker; Peter Nürnberg; Christian Kubisch; Bernd Wollnik; Abdelhamid Barakat


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
146 KB
Volume
146A
Category
Article
ISSN
1552-4825

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