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Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue
LHX4 is a LIM homeodomain transcription factor involved in the early steps of pituitary ontogenesis. To date, 8 heterozygous LHX4 mutations have been reported as responsible of combined pituitary hormone deficiency (CPHD) in Humans. We identified 4 new LHX4 heterozygous allelic variants in patients...
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| Publicado no: | PLoS One |
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| Main Authors: | , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4425544/ https://ncbi.nlm.nih.gov/pubmed/25955177 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0126648 |
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