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Severe early onset retinitis pigmentosa in a Moroccan patient with Heimler syndrome due to novel homozygous mutation of PEX1 gene

Author:

Ilham Ratbi,Imane Cherkaoui Jaouad,Hamza Elorch,Nada Al-Sheqaih,Mustapha Elalloussi,Jaber Lyahyai,Amina Berraho,William G. Newman,Abdelaziz Sefiani

Publication:

European Journal of Medical Genetics

Publisher:

Elsevier

Date:

October 2016

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