SPEG Interacts with Myotubularin, and Its Deficiency Causes Centronuclear Myopathy with Dilated CardiomyopathyPankaj B. Agrawal, Alan H. Beggs, Lindsay C. Swanson et al.|The American Journal of Human Genetics|2014Cited by 164
Normal myofibrillar development followed by progressive sarcomeric disruption with actin accumulations in a mouse Cfl2 knockout demonstrates requirement of cofilin-2 for muscle maintenancePiyush Agrawal, Alan H. Beggs, Mugdha Joshi et al.|Human Molecular Genetics|2012Cited by 89
A compound heterozygous mutation in GPD1 causes hepatomegaly, steatohepatitis, and hypertriglyceridemiaMugdha Joshi, Pankaj B. Agrawal, Jacqueline Eagan et al.|European Journal of Human Genetics|2014Cited by 54
Expanding the Phenotype Associated With the<i>NEFL</i>MutationPankaj B. Agrawal, Alan H. Beggs, Mugdha Joshi et al.|JAMA Neurology|2014Cited by 45