A rare subclinical or mild type of Becker muscular dystrophy caused by a single exon 48 deletion of the dystrophin gene

• Autorzy: Zimowski J.G. , Pilch J. , Pawelec M. , Purzycka J.K. , Kubalska J. , Ziora-Jakutowicz K. , Dudzinska M. , Zaremba J.
• Języki publikacji: EN

Abstrakty

EN

• Wydawca: -
• Czasopismo: Journal of Applied Genetics
• Rocznik: 2017
• Tom: 58
• Numer: 3
• Opis fizyczny: p.343–347,fig.,ref.

Twórcy

autor

Zimowski J.G.

• Department of Genetics, Institute of Psychiatry and Neurology, Sobieskiego 9, 02-957 Warsaw, Poland

autor

Pilch J.

• Department of Pediatrics and Neurology for Children and Adolescents, Medical University of Silesia, Medykow 16, 40-752 Katowice, Poland

autor

Pawelec M.

• Department of Genetics, Institute of Psychiatry and Neurology, Sobieskiego 9, 02-957 Warsaw, Poland

autor

Purzycka J.K.

• Department of Genetics, Institute of Psychiatry and Neurology, Sobieskiego 9, 02-957 Warsaw, Poland

autor

Kubalska J.

• Department of Genetics, Institute of Psychiatry and Neurology, Sobieskiego 9, 02-957 Warsaw, Poland

autor

Ziora-Jakutowicz K.

• Department of Genetics, Institute of Psychiatry and Neurology, Sobieskiego 9, 02-957 Warsaw, Poland

autor

Dudzinska M.

• Children’s Neurology Ward, Dr. E. Hanke Centre of Pediatrics and Oncology of Chorzow, Truchana 7, 41-500 Chorzow, Poland

autor

Zaremba J.

• Department of Genetics, Institute of Psychiatry and Neurology, Sobieskiego 9, 02-957 Warsaw, Poland

Identyfikatory

DOI

10.1007/s13353-017-0391-8