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Taylor and Francis Group, Ophthalmic Genetics, 5(43), p. 653-657, 2022

DOI: 10.1080/13816810.2022.2068045

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High myopia and vitreal veils in a patient with Poretti– Boltshauser syndrome due to a novel homozygous LAMA1 mutation

Distributing this paper is prohibited by the publisher
Distributing this paper is prohibited by the publisher

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