A novel compound heterozygous variant identified in GLDC gene in a Chinese family with non-ketotic hyperglycinemia
Abstract Background Non-ketotic hyperglycinemia (NKH) is a rare, devastating autosomal recessive disorder of glycine metabolism with a very poor prognosis. Currently, few studies have reported genetic profiling of Chinese NKH patients. This study aimed to identify the genetic mutations in a Chinese...
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| Główni autorzy: | , , , |
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| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
BMC
2018-01-01
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| Seria: | BMC Medical Genetics |
| Hasła przedmiotowe: | |
| Dostęp online: | http://link.springer.com/article/10.1186/s12881-017-0517-1 |
| Etykiety: |
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