Identification of a novel deletion in the MMAA gene in two Iranian siblings with vitamin B12-responsive methylmalonic acidemia

• Autorzy: Keyfi F. , Abbaszadegan M.R. , Rolfs A. , Orolicki S. , Moghaddassian M. , Varasteh A.
• Języki publikacji: EN

Abstrakty

EN

• Wydawca: -
• Czasopismo: Cellular and Molecular Biology Letters
• Rocznik: 2016
• Tom: 21
• Opis fizyczny: p.2-8,fig.,ref.

Twórcy

autor

Keyfi F.

• Immunology Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
• Pardis Clinical and Genetic Laboratory, Mashhad, Iran

autor

Abbaszadegan M.R.

• Division of Human Genetics, Immunology Research Center, Avicenna Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran
• Pardis Clinical and Genetic Laboratory, Mashhad, Iran

autor

Rolfs A.

• Director of the Albrecht Kossel Institute for Neuroregeneration, University of Rostock, Rostock, Germany
• Chief Medical Director, Centogene AG, Rostock, Germany

autor

Orolicki S.

• Clinical and medical scientist, Centogene AG, Rostock, Germany

autor

Moghaddassian M.

• Division of Human Genetics, Immunology Research Center, Avicenna Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran

autor

Varasteh A.

• Allergy Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
• Pardis Clinical and Genetic Laboratory, Mashhad, Iran

Identyfikatory

DOI

10.1186/s11658-016-0005-1