A molecular genetics view on Mucopolysaccharidosis Type II

Author:

Verma Shalja,Pantoom SupansaORCID,Petters Janine,Pandey Anand KumarORCID,Hermann AndreasORCID,Lukas JanORCID

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Genetics

Reference191 articles.

1. European Federation of Pharmaceutical Industries and Associations (EFPIA), (2020) https://www.efpia.eu/news-events/the-efpia-view/blog-articles/26102017-hunter-syndrome-mucopolysaccharidosis-type-ii-eu-incentives-behind-omps/ (Accessed on 20 January 2020).

2. A rare disease in two brothers;Hunter;Proc. R. Soc. Med.,1917

3. Gargoylism (Hunter-Hurler disease, dysostosis multiplex, lipochondrodystrophy); prenatal and neonatal bone lesions and their early postnatal evolution;Caffey;Bull. Hosp. Joint Dis.,1951

4. Hereditary disorders of connective tissue;McKusick;Bull. N. Y. Acad. Med.,1959

5. Inguinal hernia in the HurlerHunter syndrome;Coran;Surgery,1967

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