A homozygous intronic branch-point deletion in the ALPL gene causes infantile hypophosphatasia
Author:
Publisher
Elsevier BV
Subject
Histology,Physiology,Endocrinology, Diabetes and Metabolism
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3. Biochemical, clinical and genetic characteristics in adults with persistent hypophosphatasaemia; Data from an endocrinological outpatient clinic in Denmark;Bone Reports;2021-12
4. Case Report: Variations in the ALPL Gene in Chinese Patients With Hypophosphatasia;Frontiers in Genetics;2021-10-12
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