Severe early onset retinitis pigmentosa in a Moroccan...

European Journal of Medical Genetics 2016 / 10 Vol. 59; Iss. 10

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

Ratbi, Ilham, Jaouad, Imane Cherkaoui, Elorch, Hamza, Al-Sheqaih, Nada, Elalloussi, Mustapha, Lyahyai, Jaber, Berraho, Amina, Newman, William G., Sefiani, Abdelaziz
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Volume:
59
Language:
english
Journal:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2016.09.004
Date:
October, 2016
File:
PDF, 7.14 MB
english, 2016
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