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Novel mutations ofMYO15Aassociated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome

✍ Scribed by Nikki Liburd; Manju Ghosh; Saima Riazuddin; Sadaf Naz; Shaheen Khan; Zubair Ahmed; Sheikh Riazuddin; Yong Liang; Puthezhath S. Menon; Tenesha Smith; Ann C. Smith; Ken-Shiung Chen; James R. Lupski; Edward R. Wilcox; Lorraine Potocki; Thomas B. Friedman


Publisher
Springer
Year
2001
Tongue
English
Weight
172 KB
Volume
109
Category
Article
ISSN
0340-6717

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