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Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma

✍ Scribed by Gabriela Richard; Thomas W. White; Lisa E. Smith; Regina A. Bailey; John G. Compton; David L. Paul; S. J. Bale


Book ID
106137044
Publisher
Springer
Year
1998
Tongue
English
Weight
252 KB
Volume
103
Category
Article
ISSN
0340-6717

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