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Literature DB >> 29396812

Replay to: Phenotypic spectrum of POLG1 mutations.

Elena Cardaioli¹, Paola Da Pozzo², Antonio Federico².

Abstract

Entities: Gene

Mesh：

Substances：

Year: 2018 PMID： 29396812 DOI： 10.1007/s10072-017-3229-6

Source DB: PubMed Journal: Neurol Sci ISSN： 1590-1874 Impact factor: 3.307

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3 in total

1. Mitochondrial myopathy presenting with segmental corneal oedema and retrocorneal membrane.

Authors: Marcus H Colyer; Kraig S Bower; Thomas P Ward; Ahmad A Hidayat; Prem S Subramanian
Journal: Br J Ophthalmol Date: 2007-05 Impact factor: 4.638

2. Novel POLG mutations and variable clinical phenotypes in 13 Italian patients.

Authors: Paola Da Pozzo; Elena Cardaioli; Anna Rubegni; Gian Nicola Gallus; Alessandro Malandrini; Alessandra Rufa; Carla Battisti; Maria Alessandra Carluccio; Raffaele Rocchi; Fabio Giannini; Amedeo Bianchi; Michelangelo Mancuso; Gabriele Siciliano; Maria Teresa Dotti; Antonio Federico
Journal: Neurol Sci Date: 2017-01-27 Impact factor: 3.307

3. Phenotypic spectrum of POLG1 mutations.

Authors: Josef Finsterer; Fulvio A Scorza
Journal: Neurol Sci Date: 2017-09-13 Impact factor: 3.307

3 in total