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
Frontiers | DNAJC12 as a Mediator Between ESR1 and ERBB4 in Breast Carcinoma Cells
DNAJC12 deficiency: A new strategy in the diagnosis of hyperphenylalaninemias - ScienceDirect
Anti-DNAJC12 antibody (ab254762) | Abcam
Tissue expression of DNAJC12 - Summary - The Human Protein Atlas
Pathogenic variants of DNAJC12 and evaluation of the encoded cochaperone as a genetic modifier of hyperphenylalaninemia
Effect of DNAJC12 overexpression on expression of various genes. (A)... | Download Scientific Diagram
Heterogeneous clinical spectrum of DNAJC12-deficient hyperphenylalaninemia: from attention deficit to severe dystonia and intellectual disability | Journal of Medical Genetics
DNAJC12 promotes lung cancer growth by regulating the activation of β‑catenin
DNAJC12-associated developmental delay, movement disorder, and mild hyperphenylalaninemia identified by whole-exome sequencing re-analysis | European Journal of Human Genetics
DNAJC12 Antibody (ABIN7266822)
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability. | Semantic Scholar