Homozygosity for TNSALP mutation 1348c>T (Arg433Cys) causes infantile hypophosphatasia manifesting transient disease correction and variably lethal outcome in a kindred of black ancestry
- 30 June 2006
- journal article
- review article
- Published by Elsevier BV in The Journal of Pediatrics
- Vol. 148 (6), 753-758
- https://doi.org/10.1016/j.jpeds.2006.01.031
Abstract
No abstract availableKeywords
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