P. Anthony Akkari

A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

Nigel G. Laing, Steve D. Wilton, P. Anthony Akkari et al. · Nature Genetics · 1995 · 355 citations

Autoimmune Disease, Genetic Disorder, Medicine +3

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

Katarina Pelin, Pirta Hilpelä, Kati Donner et al. · Proceedings of the National Academy of Sciences · 1999 · 328 citations · Full text

Altered Gut Microbiome in Parkinson’s Disease and the Influence of Lipopolysaccharide in a Human α-Synuclein Over-Expressing Mouse Model

Anastazja M. Gorecki, Leah Preskey, Megan C. Bakeberg et al. · Frontiers in Neuroscience · 2019 · 182 citations · Full text

Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families

Lianna Ishihara, Rachel A. Gibson, Liling Warren et al. · Movement Disorders · 2006 · 91 citations

Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I.

Nigel G. Laing, Bernadette T. Majda, P. Anthony Akkari et al. · PubMed · 1992 · 70 citations