HE
Hamza ELORCH

Publications (4)

Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report
Article scientifique · 2021
Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report
Article scientifique · 2020
Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy
Article scientifique · 2020
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly
Article scientifique · 2019

Domaines principaux

Sciences de la santé3 Sciences de la vie et biotechnologies1

Statistiques

Consultations19
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