A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy (Q34340905)
Jump to navigation
Jump to search
scientific article
Language | Label | Description | Also known as |
---|---|---|---|
English | A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy |
scientific article |
Statements
1 reference
A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy (English)
1 reference
G Eda Utine
1 reference
Göknur Haliloğlu
1 reference
Bilge Salanci
1 reference
Arda Çetinkaya
1 reference
P Özlem Kiper
1 reference
Yasemin Alanay
1 reference
Dilek Aktas
1 reference
Koray Boduroğlu
1 reference
Mehmet Alikaşifoğlu
1 reference
22 April 2013
1 reference
1 reference
28
1 reference
7
1 reference
926-932
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference