Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome (Q34104260)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome |
scientific article |
Statements
1 reference
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome (English)
1 reference
Liburd N
1 reference
Ghosh M
1 reference
Riazuddin S
1 reference
Naz S
1 reference
Khan S
1 reference
Ahmed Z
1 reference
Riazuddin S
1 reference
Liang Y
1 reference
Menon PS
1 reference
Smith T
1 reference
Smith AC
1 reference
Chen KS
1 reference
Lupski JR
1 reference
Wilcox ER
1 reference
Potocki L
1 reference
Friedman TB
1 reference
3 October 2001
1 reference
1 reference
109
1 reference
535-541
1 reference
Identifiers
1 reference
1 reference