טוען...
Deciphering the modifiers for phenotypic variability of X-linked adrenoleukodystrophy
X-linked adrenoleukodystrophy (X-ALD), an inborn error of peroxisomal β-oxidation, is caused by defects in the ATP Binding Cassette Subfamily D Member 1 (ABCD1) gene. X-ALD patients may be asymptomatic or present with several clinical phenotypes varying from severe to mild, severe cerebral adrenoleu...
שמור ב:
| הוצא לאור ב: | World J Biol Chem |
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| Main Authors: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Baishideng Publishing Group Inc
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7672940/ https://ncbi.nlm.nih.gov/pubmed/33274015 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4331/wjbc.v11.i3.99 |
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