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FGD1 gene

Known as: FGD1, FYVE, RhoGEF and PH domain containing 1, ZFYVE3 
National Institutes of Health

Papers overview

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2017
2017
BackgroundThe X-linked condition “Aarskog-Scott syndrome (AAS)” causes a characteristic combination of short stature, facial… 
2015
2015
Aarskog–Scott syndrome (AAS), also known as faciogenital dysplasia (FGD, OMIM # 305400), is an X‐linked disorder of recessive… 
2014
2014
We present a male patient with sporadic Aarskog syndrome, cleft palate, mild intellectual disability, and autism spectrum… 
2013
2013
Frequent somatic mutations in the GNA11, matrix metalloproteinase (MMP)27, FGD1, TRRAP and GRM3 genes have been reported in… 
Highly Cited
1998
Highly Cited
1998
We purified from rat brain a novel F-actin-binding protein with a M r of about 105,000 (p105), which was estimated by SDS…