A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome. (Q64900897)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome. |
scientific article |
Statements
A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome. (English)
1 reference
H Kobayashi
1 reference
M Kasahara
1 reference
M Hino
1 reference
S Takahara
1 reference
K Ikeda
1 reference
C Son
1 reference
T Iwakura
1 reference
A Yoshimoto
1 reference
T Ishihara
1 reference
Y Ogawa
1 reference
1 October 2006
1 reference
29
1 reference
9
1 reference
851-853
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