|
🐜
|
LMNA mutations in atypical Werner's syndrome
13 auth.
Li-shan Chen,
Lin Lee,
B. Kudlow,
H. D. Santos,
O. Sletvold,
Y. Shafeghati,
Eleanor G. Botha,
A. Garg,
N. B. Hanson,
G. Martin,
...
I. Mian,
B. Kennedy,
J. Oshima
|
7 |
2003 |
7
🐜
|
|
🐜
|
Identification of mutations in CUL7 in 3-M syndrome
28 auth.
C. Huber,
D. Dias-Santagata,
A. Glaser,
J. O’Sullivan,
R. Brauner,
Kenneth Wu,
Xinsong Xu,
K. Pearce,
Rong Wang,
M. L. Uzielli,
N. Dagoneau,
W. Chemaitilly,
A. Superti-Furga,
H. D. Santos,
A. Mégarbané,
...
G. Morin,
G. Gillessen‐Kaesbach,
R. Hennekam,
I. Burgt,
G. Black,
P. Clayton,
A. Read,
M. Merrer,
P. Scambler,
A. Munnich,
Z. Pan,
R. Winter,
V. Cormier-Daire
|
7 |
2005 |
7
🐜
|
|
🐜
|
Role of Scl39a13/ZIP13 in cardiovascular homeostasis
16 auth.
Takafumi Hara,
Ikuko Yamada,
Takuto Ohashi,
Masaru Tamura,
A. Hijikata,
Takashi Watanabe,
Minghao Gao,
Kana Ito,
S. Kawamata,
Shiori Azuma,
...
E. Yoshigai,
Yukiko Sumiyoshi,
Natsumi Yasuhiro,
O. Ohara,
H. D. Santos,
T. Fukada
|
2 |
2022 |
2
🐜
|
|
🐜
|
LMNA mutations identify a new genetic subset of subjects with progeroid features of werner syndrome
12 auth.
Li-shan Chen,
Lin Lee,
B. Kudlow,
H. D. Santos,
O. Sletvold,
Y. Shafeghati,
...
Eleanor G. Botha,
A. Garg,
N. B. Hanson,
G. Martin,
I. Mian,
B. Kennedy
|
0 |
2003 |
0
🐜
|
