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A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene

✍ Scribed by Guilford, Parry; Ayadi, Hamadi; Blanchard, Stéphane; Chaib, Hassan; Paslier, Denis Le; Weissenbach, Jean; Drira, Mohamed; Petit, Christine


Book ID
121434544
Publisher
Oxford University Press
Year
1994
Tongue
English
Weight
533 KB
Volume
3
Category
Article
ISSN
0964-6906

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## Abstract The association of retinitis pigmentosa (RP) and microphthalmia has been reported in a number of familial and isolated cases. Here, the results of genetic analysis in a familial case of early RP associated with nanophthalmos are described. Two affected sibs were ascertained from an endo