טוען...
Multiple mutations are responsible for the high frequency of metachromatic leukodystrophy in a small geographic area.
Metachromatic leukodystrophy is a lysosomal storage disorder caused by the deficiency of arylsulfatase A. The disease occurs panethnically, with an estimated frequency of 1/40,000. Metachromatic leukodystrophy was found to be more frequent among Arabs living in two restricted areas in Israel. Ten fa...
שמור ב:
Main Authors: | , , , |
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פורמט: | Artigo |
שפה: | Inglês |
יצא לאור: |
1995
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נושאים: | |
גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1801341/ https://ncbi.nlm.nih.gov/pubmed/7825603 |
תגים: |
הוספת תג
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