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PBS Changes From 1 May 2024
Gene Linked to Retinitis Pigmentosa Ciliary Pathology Found
Broad Range of Solid Tumors Linked to Colorectal Cancer Gene
ALG6 Identified as Modifier Gene in Retinitis Pigmentosa 59
Sequencing Genomes of Blue Whale, Etruscan Shrew Complete
Examining Neuron Roles in STXBP1 Encephalopathy
Discovery unravels mystery of rare bone disease
New Workflow Enhances Detection of 5q-Spinal Muscular Atrophy
Single Dose of Gene-Editing Drug May Tame Inherited High LDL
New Gene Discovery Bolsters Fight Against Grape Mildew
Vascular Aging Worsens with Reduced DNA Break Repair
NICER approach to genome editing
NICER Method Revolutionizes Genome Editing
AMP Biosynthesis Vital for Longevity and Metabolic Health in Vertebrates
Scientists investigate maintenance of ancient chromosomal inversion as fuel evolution
Study examines possible role of KIF5A gene in ALS
Gene Supplementation Assessed in Mouse Model of Retinitis Pigmentosa
High-Efficiency Assay Offers Rapid Mitochondrial Disease Diagnosis
New Discovery Reveals Common Disease Pathway & Treatment Target
New Genetic Variant Found to Protect Against Alzheimer's Disease
New Treatment Emerges for Children with Long COVID and Recurrent Fever
Mayo Clinic: Severe Obesity + Genetic Variant Raise Hypertension Risk
Michael J. Fox and Shake It Up fund scientist's research
Deadly Risk for Cats: Common Heartworm, Antiparasitic Meds
BGI Reports Rare Skin Mutation Gene by Exome Sequencing
Mutation Affects Protein Movements in Autism Cases
Novel Treatment Method for Common Neuromuscular Disorder Developed
New STAT1-us quo? Novel STAT1 variants cause MSMD
Mutations in CCIN cause teratozoospermia and male infertility
Canine distemper virus drives selection for black-coated wolves
Honeycrisp genome will help scientists breed better apples
HoFH children miss out on decades of life-saving
Zinc could treat rare genetic disorder
Researchers discover dozens of genetic defects important for immune defence
Cystic fibrosis: Causal treatment suitable from childhood
"Soft" CRISPR may offer a new fix for genetic defects
Researchers survey landscape of rare mutations behind neurodegenerative diseases in Colombia
Award for research on Rett syndrome
Screening Program Could Identify 1 Million Americans with Genetic Heart Disease
Research provides new insights into genetics of heritable traits
Scientists elucidate novel molecular mechanism of MYBPC3-related hypertrophic cardiomyopathy using human iPSC-CM model
Sperm-storing tree skinks are 'secret swingers': new research
Litchi genome tells colorful story about colorful tropical fruit
PKU School of Stomatology reports new phenotype of LRP6 mutation
New recessive neurodevelopmental disorder identified
Novel Inhibitor Discovered for B-cell Lymphomas Treatment
Methylglyoxal detoxification deficits causes schizophrenia-like behavioral abnormalities
Researchers Quantify Thermodynamic Interplay during Protein Co-aggregation