Eyal Seroussi
Biographic Data
| ID | 10577473 |
|---|---|
| NAME | Eyal Seroussi |
| GIVEN NAMES | Eyal |
| FAMILY NAME | Seroussi |
| SIGNATURE | SEROUSSI E |
| AFFILIATIONS | Tel Aviv University |
| ORCID | 0000-0001-6191-8948 |
| VERIFIED | Yes |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 1 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 1997 |
| LATEST PUBLICATION YEAR | 1997 |
| H-INDEX | 0 |
Usher syndrome in the Samaritans
We have previously reported significant linkage between markers on 11q13.5 and Usher syndrome type 1 (USH1B) in a large Samaritan kindred. USH1B is an autosomal recessive disease characterized by profound congenital sensorineural deafness, vestibular dysfunction and progressive visual loss. A unique haplotype found only in all USH1B carriers and affected individuals implied that the disease-causing mutation probably entered the community from a s…
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Usher syndrome in the Samaritans
We have previously reported significant linkage between markers on 11q13.5 and Usher syndrome type 1 (USH1B) in a large Samaritan kindred. USH1B is an autosomal recessive disease characterized by profound congenital sensorineural deafness, vestibular dysfunction and progressive visual loss. A unique haplotype found only in all USH1B carriers and affected individuals implied that the disease-causing mutation probably entered the community from a s…
Allele (1 work) · Biochemical Analysis and Sensing Techniques (1 work) · Biology (1 work) · Gene (1 work) · Genetic linkage (1 work) · Genetics (1 work) · Haplotype (1 work) · Hearing loss (1 work) · Hearing, Cochlea, Tinnitus, Genetics (1 work) · Medicine (1 work)