Rebecca S. Greenleaf

Nemaline myopathy with minicores caused by mutation of the CFL2 gene encoding the skeletal muscle actin-binding protein, cofilin-2.

P. Dormitzer, V. Lehtokari, A. Beggs, 2007, American journal of human genetics.

The exon 55 deletion in the nebulin gene – One single founder mutation with world-wide occurrence

K. Pelin, V. Lehtokari, A. Beggs, 2009, Neuromuscular Disorders.

Innovations in Maternal and Child Health: Pairing Undergraduate and Graduate Maternal and Child Health Students in Summer Practica in State Title V Agencies

Deneen N. Long-White, A. Handler, D. Cilenti, 2018, Maternal and Child Health Journal.

Mutation spectrum in the large GTPase dynamin 2, and genotype–phenotype correlation in autosomal dominant centronuclear myopathy

Jocelyn Laporte, Luciano Merlini, Christophe Béroud, 2012, Human mutation.