J. Stajich

Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

F. Baas, S. Züchner, J. Vance, 2006, Annals of neurology.

Recombinant DNA strategies in genetic neurological diseases

M. Pericak-Vance, A. Roses, J. Vance, 1983, Muscle & nerve.

Exome sequencing detection of two untranslated GFPT1 mutations in a family with limb‐girdle myasthenia

Q. Yi, R. Maselli, R. Wollmann, 2014, Clinical genetics.

Stargardt ' s Type Maculopathy in a Patient with 11778 Leber ' s Optic Neuropathy

E. W. Brown, M. Pericak-Vance, S. Brodie, 2019 .

Cardiac Involvement in Myotonic Muscular Dystrophy

R. Coleman, A. Roses, D. Packer, 1985, Medicine.