Detection of deletion 1154-1156 hypophosphatasia mutation using TNSALP exon amplification
about
HypophosphatasiaPathophysiology of hypophosphatasia and the potential role of asfotase alfaHypophosphatasia: the mutations in the tissue-nonspecific alkaline phosphatase geneChoice of Feeders Is Important When First Establishing iPSCs Derived From Primarily Cultured Human Deciduous Tooth Dental Pulp CellsPossible interference between tissue-non-specific alkaline phosphatase with an Arg54-->Cys substitution and acounterpart with an Asp277-->Ala substitution found in a compound heterozygote associated with severe hypophosphatasia.Skeletal mineralization defects in adult hypophosphatasia--a clinical and histological analysis.Perinatal hypophosphatasia presenting as neonatal epileptic encephalopathy with abnormal neurotransmitter metabolism secondary to reduced co-factor pyridoxal-5'-phosphate availability.Molecular and clinical analysis of ALPL in a cohort of patients with suspicion of Hypophosphatasia.
P2860
Q21202964-0E6C2969-547E-4ED3-8CAB-0EC2491C8C7DQ26747780-283FADD0-B91B-43F2-B563-E7FC4890FB3EQ28140030-C9C7BA0D-A91F-474E-9DFC-36C01990BEC7Q36523729-E6CAD9B7-0EB9-4318-832D-F2E19EB66376Q41853551-B62ED06F-B88E-443B-8D61-0EA64B7CA9FAQ46294748-8BB00B95-7540-4C7F-BDCB-17EEA50CB748Q48356405-E89F8AF6-523D-4E20-BE4A-EEE1BB64FFE6Q53739961-1EF558C8-022F-44E0-8FA6-2E2663474B7E
P2860
Detection of deletion 1154-1156 hypophosphatasia mutation using TNSALP exon amplification
description
1997 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի հունիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1997
@ast
im Juni 1997 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: June 1997)
@en
vedecký článok (publikovaný 1997/06/01)
@sk
vědecký článek publikovaný v roce 1997
@cs
wetenschappelijk artikel (gepubliceerd op 1997/06/01)
@nl
наукова стаття, опублікована в червні 1997
@uk
научни чланак (објављен 1997/06/01)
@sr
name
Detection of deletion 1154-1156 hypophosphatasia mutation using TNSALP exon amplification
@ast
Detection of deletion 1154-1156 hypophosphatasia mutation using TNSALP exon amplification
@en
Detection of deletion 1154-1156 hypophosphatasia mutation using TNSALP exon amplification
@nl
type
label
Detection of deletion 1154-1156 hypophosphatasia mutation using TNSALP exon amplification
@ast
Detection of deletion 1154-1156 hypophosphatasia mutation using TNSALP exon amplification
@en
Detection of deletion 1154-1156 hypophosphatasia mutation using TNSALP exon amplification
@nl
prefLabel
Detection of deletion 1154-1156 hypophosphatasia mutation using TNSALP exon amplification
@ast
Detection of deletion 1154-1156 hypophosphatasia mutation using TNSALP exon amplification
@en
Detection of deletion 1154-1156 hypophosphatasia mutation using TNSALP exon amplification
@nl
P2093
P3181
P356
P1433
P1476
Detection of deletion 1154-1156 hypophosphatasia mutation using TNSALP exon amplification
@en
P2093
P3181
P356
10.1006/GENO.1997.4733
P407
P577
1997-06-01T00:00:00Z