Author

Mohamed Zarhrate

Institutions: Hôpital Necker-Enfants Malades, Inserm, Institut Necker Enfants Malades, Assistance Publique – Hôpitaux de Paris

Observed institutions: Hôpital Necker-Enfants Malades, Inserm, Institut Necker Enfants Malades, Assistance Publique – Hôpitaux de Paris

OpenAlex ID: A5079848639

Mitochondrial DNA Depletion is a Prevalent Cause of Multiple Respiratory Chain Deficiency in Childhood

2007 · Emmanuelle Sarzi, Alice Bourdon, et al. · The Journal of Pediatrics · 163

Incidence and clinical features of X-linked Cornelia de Lange syndrome due toSMC1L1 mutations

2007 · Guntram Borck, Mohamed Zarhrate, et al. · Human Mutation · 75

Father-to-daughter transmission of Cornelia de Lange syndrome caused by a mutation in the 5′ untranslated region of theNIPBL Gene

2006 · Guntram Borck, Mohamed Zarhrate, et al. · Human Mutation · 61

Works count: 3

Citation count: 299

H-index: 3

I10-index: 3