Hunter Syndrome
| dc.contributor.author | Mohammed, Bouthaina | |
| dc.date.accessioned | 2019-06-25T09:07:31Z | |
| dc.date.available | 2019-06-25T09:07:31Z | |
| dc.date.issued | 2018-04-14 | |
| dc.identifier.uri | http://repository.limu.edu.ly/handle/123456789/966 | |
| dc.description | Mucopolysaccharidosis type II (MPS II) is a rare X -linked recessive disorder in which the body is missing or does not have enough of an enzyme needed to break down long chains of sugar molecules, Without this enzyme, chains of sugar molecules build up in various body tissues and causing damage | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | faculty of Basic Medical Science - Libyan International Medical University | en_US |
| dc.rights | Attribution 3.0 United States | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/3.0/us/ | * |
| dc.title | Hunter Syndrome | en_US |
| dc.type | Other | en_US |
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