Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect.

Shahrour, Maher Awni; Nicolae, Claudia M; Edvardson, Simon; Ashhab, Motee; Galvan, Adri M; Constantin, Daniel; Abu-Libdeh, Bassam; Moldovan, George-Lucian; Elpeleg, Orly

Shahrour, Maher Awni; Nicolae, Claudia M; Edvardson, Simon; Ashhab, Motee; Galvan, Adri M; Constantin, Daniel; Abu-Libdeh, Bassam; Moldovan, George-Lucian; Elpeleg, Orly.

Afiliação

Shahrour MA; Department of Pediatrics, Al-Makassed Islamic Hospital, Jerusalem, Israel.
Nicolae CM; Department of Biochemistry and Molecular Biology, The Pennsylvania State University College of Medicine, Hershey, PA, 17033, USA.
Edvardson S; Pediatric Neurology Unit, Hadassah, Hebrew University Medical Center, Jerusalem, Israel.
Ashhab M; Monique and Jacques Roboh Department of Genetic Research, Hadassah, Hebrew University Medical Center, Jerusalem, Israel.
Galvan AM; Department of Pediatrics, Al-Makassed Islamic Hospital, Jerusalem, Israel.
Constantin D; Department of Biochemistry and Molecular Biology, The Pennsylvania State University College of Medicine, Hershey, PA, 17033, USA.
Abu-Libdeh B; Department of Biochemistry and Molecular Biology, The Pennsylvania State University College of Medicine, Hershey, PA, 17033, USA.
Moldovan GL; Department of Pediatrics, Al-Makassed Islamic Hospital, Jerusalem, Israel.
Elpeleg O; Department of Biochemistry and Molecular Biology, The Pennsylvania State University College of Medicine, Hershey, PA, 17033, USA. gmoldovan@hmc.psu.edu.

Neurogenetics ; 18(2): 119, 2017 04.

Article em En | MEDLINE | ID: mdl-28190220

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Neurogenetics Assunto da revista: GENETICA / NEUROLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Israel

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