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Connexin 26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans
- Authors :
- Zelante, L.
Gasparini, Paolo
Estivill, X.
Melchionda, S.
D\'Agruma, L.
Govea, N.
Milà, M.
DELLA MONICA, M.
Lutfi, J.
Shohat, M.
Mansfield, E.
L., Zelante
Gasparini, Paolo
X., Estivill
S., Melchionda
L., D\'Agruma
N., Govea
M., Milà
M., DELLA MONICA
J., Lutfi
M., Shohat
E., Mansfield
- Publication Year :
- 1997
Details
- Database :
- OpenAIRE
- Accession number :
- edsair.dedup.wf.001..379ef36b5becdc085ba59d2bbe175a0a