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Developmental Outcomes of School-Age Children with Duarte Galactosemia: A Pilot Study
Duarte galactosemia (DG) is a mild allelic variant of classic galactosemia that results from partial impairment of galactose-1P uridylyltransferase (GALT). Although infants with DG are detected by newborn screening in some US states at close to 1/4,000 live births, most are discharged from follow-up...
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| Publicado no: | JIMD Rep |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4501238/ https://ncbi.nlm.nih.gov/pubmed/25681083 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2014_370 |
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