Correction to: Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene

Affiliations

• ¹ Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt. nm.elaraby@nrc.sci.eg.
• ² Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
• ³ Genetics Department, Ain Shams University, Cairo, Egypt.
• ⁴ Pediatric Department, Maadi Hospital, Cairo, Egypt.
• ⁵ Prenatal Diagnosis and Fetal Medicine Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
• ⁶ Orodental Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
• ⁷ Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.