A COMMON MUTATION IN THE CONNEXIN-26 GENE IS THE PRIMARY CAUSE OF SPORADIC AND FAMILIAR CONGENITAL DEAFNESS IN MEDITERRANEAN POPULATIONS

ESTIVILL X RABIONET K ZELANTE L MELCHIONDA S DAGRUMA L MILA M GOVEA N DELGROSSO K SURREY S MANSFIELD E RAPPAPORT E FORTINA P GASPARINI P

X. Estivill et al., A COMMON MUTATION IN THE CONNEXIN-26 GENE IS THE PRIMARY CAUSE OF SPORADIC AND FAMILIAR CONGENITAL DEAFNESS IN MEDITERRANEAN POPULATIONS, American journal of human genetics, 61(4), 1997, pp. 108-108

NO

American journal of human genetics → ACNP

00029297

61

4

1997

S

108 - 108

ISI

0002-9297(1997)61:4<108:ACMITC>2.0.ZU;2-F