M Korostishevsky
Datos Biográficos
| ID | 5209836 |
|---|---|
| NOMBRE | M Korostishevsky |
| NOMBRES | M |
| APELLIDO | Korostishevsky |
| FIRMA | KOROSTISHEVSKY M |
| AFILIACIONES | Tel Aviv University |
| VERIFICADO | No |
| TOTAL DE OBRAS | 1 |
| TOTAL DE CITAS | 0 |
| OBRAS COMO AUTOR | 1 |
| OBRAS COMO EDITOR | 0 |
| PRIMER AÑO DE PUBLICACIÓN | 1997 |
| AÑO MÁS RECIENTE DE PUBLICACIÓN | 1997 |
| ÍNDICE H | 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 obra) · Biochemical Analysis and Sensing Techniques (1 obra) · Biology (1 obra) · Gene (1 obra) · Genetic linkage (1 obra) · Genetics (1 obra) · Haplotype (1 obra) · Hearing loss (1 obra) · Hearing, Cochlea, Tinnitus, Genetics (1 obra) · Medicine (1 obra)