The severe clinical phenotype for a heterozygous Fabry female patient correlates to the methylation of non-mutated allele associated with chromosome 10q26 deletion syndrome
| Image |  |
|---|---|
| Description | scientific article published on 7 January 2017 |
| Author/s |
author: Mohammad Arif Hossain |
| Publication date | January 7, 2017 |
| Language | English |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |