Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene (Q50518927)
Jump to navigation
Jump to search
scientific article published in August 1995
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene |
scientific article published in August 1995 |
Statements
Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene (English)
1 reference
1 reference
F Carella
1 reference
A Toscano
1 reference
P Soliveri
1 reference
P Girlanda
1 reference
F Carrara
1 reference
G M Fratta
1 reference
F M Reid
1 reference
C Mariotti
1 reference
M Zeviani
1 reference
1 August 1995
1 reference
4
1 reference
8
1 reference
1421-1427
1 reference