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Homozygous variants in the HEXB and MBOAT7 genes underlie neurological diseases in consanguineous families
BACKGROUND: Neurological disorders are a common cause of morbidity and mortality within Pakistani populations. It is one of the most important challenges in healthcare, with significant life-long socio-economic burden. METHODS: We investigated the cause of disease in three Pakistani families in indi...
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| Publicat a: | BMC Med Genet |
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| Autors principals: | , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6921424/ https://ncbi.nlm.nih.gov/pubmed/31852446 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-019-0907-7 |
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