Mutations in the protein tyrosine kinase gene, PTPN11, cause Noonan Syndrome (vol 29, pg 465, 2001)

被引:8
作者
Tartaglia, M
Mehler, EL
Goldberg, R
Zampino, G
Brunner, HG
Kremer, H
van der Burgt, I
Crosby, AH
Ion, A
Jeffery, S
Kalidas, K
Patton, MA
Kucherlapati, RS
Gelb, B
机构
关键词
D O I
10.1038/ng1201-491c
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Nature Genet. 29, 465–468 (2001)). Regrettably, we did not provide acknowledgment of two sources of funding before our paper was published online on 12 November. Full acknowledgment follows.
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页码:491 / 491
页数:1
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[1]   Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome [J].
Tartaglia, M ;
Mehler, EL ;
Goldberg, R ;
Zampino, G ;
Brunner, HG ;
Kremer, H ;
van der Burgt, I ;
Crosby, AH ;
Ion, A ;
Jeffery, S ;
Kalidas, K ;
Patton, MA ;
Kucherlapati, RS ;
Gelb, BD .
NATURE GENETICS, 2001, 29 (04) :465-468