Publications by authors named "Peter G Procopis"

Claim this Profile
A
A patient with homozygous nonsense variants in two Leigh syndrome disease genes: Distinguishing a dual diagnosis from a hypomorphic protein-truncating variant.
Nicole J Lake, Luke E Formosa, David A Stroud, Michael T Ryan, Sarah E Calvo, Peter G Procopis

Hum Mutat· July 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy.
Kavitha Kothur, Katherine Holman, Elizabeth Farnsworth, Gladys Ho, Michelle Lorentzos, Peter G Procopis

Seizure· July 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A founder mutation in PET100 causes isolated complex IV deficiency in Lebanese individuals with Leigh syndrome.
Sze Chern Lim, Katherine R Smith, David A Stroud, Alison G Compton, Elena J Tucker, Peter G Procopis

Am J Hum Genet· February 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers Syndrome.
Alison G Compton, Christopher Troedson, Meredith Wilson, Peter G Procopis, Fang-Yuan Li

Mitochondrion· January 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Evidence-based medicine.
Peter G Procopis

Dev Med Child Neurol· July 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis