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Pelerin sistem Germina phka2 Productiv psalmodiere Da naștere

A novel PHKA2 mutation in a Chinese child with glycogen storage disease  type IXa: a case report and literature review | BMC Medical Genetics | Full  Text
A novel PHKA2 mutation in a Chinese child with glycogen storage disease type IXa: a case report and literature review | BMC Medical Genetics | Full Text

PHKA2 Gene - GeneCards | KPB2 Protein | KPB2 Antibody
PHKA2 Gene - GeneCards | KPB2 Protein | KPB2 Antibody

Complete Genomic Structure and Mutational Spectrum of PHKA2 in Patients  with X-Linked Liver Glycogenosis Type I and II - ScienceDirect
Complete Genomic Structure and Mutational Spectrum of PHKA2 in Patients with X-Linked Liver Glycogenosis Type I and II - ScienceDirect

Final Diagnosis -- Case 751
Final Diagnosis -- Case 751

PHKA2 antibody (24658-1-AP) | Proteintech
PHKA2 antibody (24658-1-AP) | Proteintech

PHKA2 Antibody (N-term) MBS9207897 from MyBioSource.com | Biocompare.com
PHKA2 Antibody (N-term) MBS9207897 from MyBioSource.com | Biocompare.com

Missense mutations in the PHKA2 gene in five cases of X-linked liver... |  Download Scientific Diagram
Missense mutations in the PHKA2 gene in five cases of X-linked liver... | Download Scientific Diagram

PHKA2 Exons and Primers Used for SSCP Analysis | Download Table
PHKA2 Exons and Primers Used for SSCP Analysis | Download Table

PHKA2 Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech 20 μL;  Unconjugated Products | Fisher Scientific
PHKA2 Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech 20 μL; Unconjugated Products | Fisher Scientific

PHKA1/PHKA2 Rabbit anti-Human, Mouse, Rat, Polyclonal, Invitrogen™ 100 μL;  Unconjugated Products | Fisher Scientific
PHKA1/PHKA2 Rabbit anti-Human, Mouse, Rat, Polyclonal, Invitrogen™ 100 μL; Unconjugated Products | Fisher Scientific

PHKA2 antibody (24658-1-AP) | Proteintech
PHKA2 antibody (24658-1-AP) | Proteintech

Pathogenic variants in PHKA2, which encodes the α-subunit of the... |  Download Scientific Diagram
Pathogenic variants in PHKA2, which encodes the α-subunit of the... | Download Scientific Diagram

PHKA2 Antibody (ABIN2856594)
PHKA2 Antibody (ABIN2856594)

anti-Homo sapiens (Human) PHKA2 Antibody raised in Rabbit - Cusabio
anti-Homo sapiens (Human) PHKA2 Antibody raised in Rabbit - Cusabio

PHKA2 antibody Western SAB1406255 XLG
PHKA2 antibody Western SAB1406255 XLG

PHKA2 novel mutation. (A) The role of glycogen phosphorylase (PYGL) and...  | Download Scientific Diagram
PHKA2 novel mutation. (A) The role of glycogen phosphorylase (PYGL) and... | Download Scientific Diagram

PHKA2 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT -  Santa Cruz Biotechnology
PHKA2 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology

PHKA2 Gene - GeneCards | KPB2 Protein | KPB2 Antibody
PHKA2 Gene - GeneCards | KPB2 Protein | KPB2 Antibody

PHKA2 Antibody (F-1) | SCBT - Santa Cruz Biotechnology
PHKA2 Antibody (F-1) | SCBT - Santa Cruz Biotechnology

Addgene: PHKA2 gRNA (BRDN0001146244)
Addgene: PHKA2 gRNA (BRDN0001146244)

PHKA2-AS1 Gene - GeneCards | PHKA2-AS1 RNA Gene
PHKA2-AS1 Gene - GeneCards | PHKA2-AS1 RNA Gene

PHKA1/PHKA2 Polyclonal Antibody, Invitrogen 100 μL;  Unconjugated:Antibodies, | Fisher Scientific
PHKA1/PHKA2 Polyclonal Antibody, Invitrogen 100 μL; Unconjugated:Antibodies, | Fisher Scientific

A novel PHKA2 mutation in a Chinese child with glycogen storage disease  type IXa: a case report and literature review | BMC Medical Genetics | Full  Text
A novel PHKA2 mutation in a Chinese child with glycogen storage disease type IXa: a case report and literature review | BMC Medical Genetics | Full Text

PHKA2 Gene - GeneCards | KPB2 Protein | KPB2 Antibody
PHKA2 Gene - GeneCards | KPB2 Protein | KPB2 Antibody

PHKA2 Antibody (F-1) | SCBT - Santa Cruz Biotechnology
PHKA2 Antibody (F-1) | SCBT - Santa Cruz Biotechnology

PHKA2 mutation spectrum in Korean patients with glycogen storage disease  type IX: prevalence of deletion mutations | BMC Medical Genetics | Full Text
PHKA2 mutation spectrum in Korean patients with glycogen storage disease type IX: prevalence of deletion mutations | BMC Medical Genetics | Full Text