Φορτώνει......
Mutations in the human SIX3 gene in holoprosencephaly are loss of function
Holoprosencephaly (HPE) is the most common developmental anomaly of the human forebrain; however, the genetics of this heterogeneous and etiologically complex malformation is incompletely understood. Heterozygous mutations in SIX3, a transcription factor gene expressed in the anterior forebrain and...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Oxford University Press
2008
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2733808/ https://ncbi.nlm.nih.gov/pubmed/18791198 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn294 |
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