Salt Turbulenţă cupru dnajc12 stoc preparare perceptibil
Two novel mutations in DNAJC12 identified by whole‐exome sequencing in a patient with mild hyperphenylalaninemia - Li - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library
DNAJC12-associated developmental delay, movement disorder, and mild hyperphenylalaninemia identified by whole-exome sequencing re-analysis | European Journal of Human Genetics
DNAJC12 promotes lung cancer growth by regulating the activation of β‑catenin
Anti-DNAJC12 antibody (ab254762) | Abcam
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability. | Semantic Scholar
Frontiers | DNAJC12 as a Mediator Between ESR1 and ERBB4 in Breast Carcinoma Cells
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability
Effect of DNAJC12 overexpression on expression of various genes. (A)... | Download Scientific Diagram
DNAJC12 deficiency: A new strategy in the diagnosis of hyperphenylalaninemias - ScienceDirect
DNAJC12 Antibody (NBP1-57718): Novus Biologicals
DNAJC12 Polyclonal Antibody (12338-1-AP)
DNAJC12 Gene - GeneCards | DJC12 Protein | DJC12 Antibody
dNAJc12 expression levels are upregulated in human lung cancer tissues.... | Download Scientific Diagram
Proponen incluir un gen recientemente descrito en el cribado neonatal de la hiperfenilalaninemia | CIBERER
Heterogeneous clinical spectrum of DNAJC12-deficient hyperphenylalaninemia: from attention deficit to severe dystonia and intellectual disability | Journal of Medical Genetics
DNAJC12 deficiency: A new strategy in the diagnosis of hyperphenylalaninemias - ScienceDirect
Neurotransmitter Disorders: DNAJC12-Deficient Hyperphenylalaninemia – An Emerging Neurotransmitter Disorder (Chapter 22) - Movement Disorders and Inherited Metabolic Disorders