Dominant-negative kinase domain mutations inFGFR1can explain the clinical severity of Hartsfield syndrome-Reference-Cited by-同舟云学术

Dominant-negative kinase domain mutations inFGFR1can explain the clinical severity of Hartsfield syndrome

Published:2016-02-29 Issue:10 Volume:25 Page:1912-1922
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Hong Sungkook,Hu Ping,Marino Juliana,Hufnagel Sophia B.,Hopkin Robert J.,Toromanović Alma,Richieri-Costa Antonio,Ribeiro-Bicudo Lucilene A.,Kruszka Paul,Roessler Erich,Muenke Maximilian

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/25/10/1912/18527088/ddw064.pdf

Reference42 articles.

1. The Fibroblast Growth Factor signaling pathway

2. Initiation to end point: the multiple roles of fibroblast growth factors in neural development

3. The genetics of early telencephalon patterning: some assembly required

4. FGFR1 function at the earliest stages of mouse limb development plays an indispensable role in subsequent autopod morphogenesis

5. A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

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