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Identification and diagnostic evaluation of hearing impairments in early childhood in German-speaking infants

โœ Scribed by C. Kiese-Himmel; J. Schroff; E. Kruse


Publisher
Springer-Verlag
Year
1997
Tongue
English
Weight
749 KB
Volume
254
Category
Article
ISSN
0302-9530

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Mutations in the connexin 26 gene (GJB2) are responsible for the major part of nonsyndromic autosomal recessive or apparently sporadic prelingual deafness in Caucasians (DFNB1). We screened 228 German hearing-impaired persons for mutations in the GJB2 gene by sequence analysis. Homozygous or compoun