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Table 1 Number of families participated in this study

From: Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes

Number of family

Sporadic

Autosomal dominant

Autosomal recessive

Undetermined

Nonsyndromic

41 (20)

8 (4†)

8 (2)

1‡ (0)

Syndromic

11 (3)

1 (1)

2 (1)

0 (0)

  1. Number in partenthesis indicate the families whose candidate responsible gene was narrowed down to one
  2. †Two responsible genes in 2 cases were identified in a family (family 1633)
  3. ‡Parents and proband all show hearing loss