DNAJC12 Gene - GeneCards | DJC12 Protein | DJC12 Antibody
DNAJC12 Antibody (ABIN7266822)
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability. | Semantic Scholar
Gene: DNAJC12 (ENSG00000108176) - Summary - Homo_sapiens - Ensembl genome browser 110
Elliott's Journey with DNAJC12 Deficiency - Rare Disease Day 2023
Frontiers | DNAJC12 as a Mediator Between ESR1 and ERBB4 in Breast Carcinoma Cells
Frontiers | DNAJC12 as a Mediator Between ESR1 and ERBB4 in Breast Carcinoma Cells
DNAJC12-associated developmental delay, movement disorder, and mild hyperphenylalaninemia identified by whole-exome sequencing re-analysis | European Journal of Human Genetics
DnaJC12 siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
Proponen incluir un gen recientemente descrito en el cribado neonatal de la hiperfenilalaninemia | CIBERER
DNAJC12 Polyclonal Antibody (12338-1-AP)
IHCeasy DNAJC12 Ready-To-Use IHC Kit KHC0414 | Proteintech
dNAJc12 expression levels are upregulated in human lung cancer tissues.... | Download Scientific Diagram
DNAJC12 and dopa‐responsive nonprogressive parkinsonism - Straniero - 2017 - Annals of Neurology - Wiley Online Library
DNAJC12 promotes lung cancer growth by regulating the activation of β‑catenin
DnaJ/HSP40 Homolog Subfamily C, Member 12 (DNAJC12) Protein | Abbexa Ltd
Heterogeneous clinical spectrum of DNAJC12-deficient hyperphenylalaninemia: from attention deficit to severe dystonia and intellectual disability | Journal of Medical Genetics
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability
DNAJC12 deficiency: A new strategy in the diagnosis of hyperphenylalaninemias - ScienceDirect
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability. | Semantic Scholar
DNAJC12 antibody (12338-1-AP) | Proteintech
