Klin Padiatr 2021; 233(05): e3
DOI: 10.1055/a-1493-1168
Correction: Tay-Sachs Disease: Two Novel Rare HEXA Mutations from Pakistan and Morocco
Authors
-
Farah Bibi
1
Institute of Biochemistry and Biotechnology, Pir Mehar Ali Shah Arid Agriculture University,
Rawalpindi, Pakistan
-
Asmat Ullah
2
Department of Molecular Biology, Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad,
Pakistan
-
Thomas Bourinaris
3
Department of Neuromuscular disorders, UCL Queen Square Institute of Neurology, London,
United Kingdom
-
Stephanie Efthymiou
3
Department of Neuromuscular disorders, UCL Queen Square Institute of Neurology, London,
United Kingdom
-
Yamna Kriouile
4
Unit of Neuropediatrics and Neurometabolism, Pediatric Department, Mohammed V University
of Rabat, Morocco
-
Tipu Sultan
5
The Children’s Hospital, Institute of Child Health, Islamabad, Pakistan
-
Shahzad Haider
6
Izzat Ali Shah Hospital, Lalarukh Wah Cantt, Rawalpindi, Pakistan
-
Vincenzo Salpietro
3
Department of Neuromuscular disorders, UCL Queen Square Institute of Neurology, London,
United Kingdom
-
Henry Houlden
3
Department of Neuromuscular disorders, UCL Queen Square Institute of Neurology, London,
United Kingdom
-
Ghazala Kaukab Raja
1
Institute of Biochemistry and Biotechnology, Pir Mehar Ali Shah Arid Agriculture University,
Rawalpindi, Pakistan
Erratum
Farah Bibi, Asmat Ullah, Thomas Bourinaris, Stephanie
Efthymiou, Yamna Kriouile, Shahzad Haider, Tipu Sultan,
Vincenzo Salpietro, Henry Houlden, Ghazala Kaukab Raja.
Tay-Sachs Disease: Two Novel Rare HEXA Mutations from
Pakistan and Morocco.
Klin Padiatr 2021;233
DOI: 10.1055/a-1371-1561
In the above mentioned article figure 1 was missing.
Publication History
Article published online:
10 May 2021
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