S. Rahman

A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat.

M. Siciliano, R. Krahe, C. Winchester, 1995, Human molecular genetics.

Decrease of 3243 A-->G mtDNA mutation from blood in MELAS syndrome: a longitudinal study.

S. Rahman, A. Suomalainen, J. Poulton, 2001, American journal of human genetics.

A Study into the Evolutionary Divergence of the Core Promoter Elements of PRPF31 and TFPT

Amna Z. Shah, S. Bhattacharya, G. Alfano, 2013, Journal of Molecular and Genetic Medicine.

Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

I. Nelson, N. Wood, S. Heales, 1998, American journal of human genetics.

A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy.

I. Nelson, J. Cooper, A. Schapira, 1999, American journal of human genetics.