IJMS | Free Full-Text | Clinical and Genetic Characteristics of Pediatric Patients with Hypophosphatasia in the Russian Population
A novel missense mutation in the ALPL gene causes dysfunction of the protein
ALPL Gene - GeneCards | PPBT Protein | PPBT Antibody
Two Novel Mutations in the ALPL gene of Unrelated Chinese Children with Hypophosphatasia: Case Reports and Literature Review
Epidemiological, Clinical and Genetic Study of Hypophosphatasia in A Spanish Population: Identification of Two Novel Mutations in The Alpl Gene | Scientific Reports
Investigation of ALPL variant states and clinical outcomes: An analysis of adults and adolescents with hypophosphatasia treated
ALPL Gene - GeneCards | PPBT Protein | PPBT Antibody
Clinical and genetic characteristics of hypophosphatasia in Chinese children | Orphanet Journal of Rare Diseases | Full Text
A missense change in the canine ALPL gene. (a) Sequence chromatograms... | Download Scientific Diagram
Cells | Free Full-Text | Tissue-Nonspecific Alkaline Phosphatase, a Possible Mediator of Cell Maturation: Towards a New Paradigm
Two novel mutations in the ALPL gene of unrelated Chinese children with Hypophosphatasia: case reports and literature review | BMC Pediatrics | Full Text
Cell biology: The role of the alkaline phosphatase (Alpl) gene in preventing premature bone ageing
Study design. ALP alkaline phosphatase; ALPL-positive genetically... | Download Scientific Diagram
ALPL Gene - GeneCards | PPBT Protein | PPBT Antibody
A Genetic Overview of Hypophosphatasia
Dissecting Mutational Allosteric Effects in Alkaline Phosphatases Associated with Different Hypophosphatasia Phenotypes: An Integrative Computational Investigation | bioRxiv
A novel missense mutation in the ALPL gene causes dysfunction of the protein
Epidemiological, Clinical and Genetic Study of Hypophosphatasia in A Spanish Population: Identification of Two Novel Mutations in The Alpl Gene | Scientific Reports
Frontiers | Case Report: Variations in the ALPL Gene in Chinese Patients With Hypophosphatasia
Flowchart visualising the inclusion and recruitment process of the... | Download Scientific Diagram
Clinical and genetic characteristics of hypophosphatasia in Chinese children | Orphanet Journal of Rare Diseases | Full Text
A compound heterozygous mutation of the alkaline phosphatase ALPL gene causes hypophosphatasia in a Han Chinese family
Cells | Free Full-Text | Tissue-Nonspecific Alkaline Phosphatase, a Possible Mediator of Cell Maturation: Towards a New Paradigm
