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UnknownDefining the phenotype of PGAP3-congenital disorder of glycosylation; a review of 65 cases.
Not available
S-EPMC10872732 | biostudies-literature
UnknownContribution of PGAP3 co-amplified and co-overexpressed with ERBB2 at 17q12 involved poor prognosis in gastric cancer.
Not available
S-EPMC10424286 | biostudies-literature
UnknownA novel PGAP3 mutation in a Croatian boy with brachytelephalangy and a thin corpus callosum.
Not available
S-EPMC5842148 | biostudies-literature
UnknownPGAP3 is expressed at increased levels in asthmatic ASM and is associated with increased ASM proliferation, contractility and expression of GATA3 and ALOX5.
Not available
S-EPMC11936287 | biostudies-literature
UnknownA Treatable Cause of Seizures and Hyperphosphatasia: Patients with PGAP2 and PGAP3 Mutations.
Not available
S-EPMC12503530 | biostudies-literature
UnknownA Novel PGAP3 Gene Mutation-Related Megalocornea Can Be Misdiagnosed as Primary Congenital Glaucoma.
Not available
S-EPMC9585391 | biostudies-literature
UnknownPGAP3 Associated with Hyperphosphatasia with Mental Retardation Plays a Novel Role in Brain Morphogenesis and Neuronal Wiring at Early Development.
Not available
S-EPMC7569840 | biostudies-literature
UnknownMutations in PGAP3 impair GPI-anchor maturation, causing a subtype of hyperphosphatasia with mental retardation.
Not available
S-EPMC3928656 | biostudies-literature
UnknownHyperphosphatasia with Mental Retardation Syndrome Due to a Novel Mutation in PGAP3.
Not available
S-EPMC5548534 | biostudies-literature
UnknownBilateral Glaucoma as Possible Additional Feature for PGAP3-Associated Hyperphosphatasia.
Not available
S-EPMC10981546 | biostudies-literature
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