Functional analysis of GALT variants found in classic galactosemia patients using a novel cell‐free translation method - Canson - 2019 - JIMD Reports - Wiley Online Library
The natural history of classic galactosemia: lessons from the GalNet registry | Orphanet Journal of Rare Diseases | Full Text
Screening for galactosemia: is there a place for it? | IJGM
Molecular dynamics, residue network analysis, and cross-correlation matrix to characterize the deleterious missense mutations in GALE causing galactosemia III | SpringerLink
The natural history of classic galactosemia: lessons from the GalNet registry | Orphanet Journal of Rare Diseases | Full Text
Galactosemia case presentation
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Galactosemia causes, symptoms, diagnosis, treatment & galactosemia diet
Galactosemia, a Single Gene Disorder With Epigenetic Consequences | Pediatric Research
Milk or no milk? Study fills long‑time knowledge gap on babies with genetic disorder – WSU Insider
Primary ovarian insufficiency in classic galactosemia: current understanding and future research opportunities | SpringerLink
Screening for galactosemia: is there a place for it? - Abstract - Europe PMC
pediatrics Flashcards | Quizlet
Galactosemia by Farshid Mokhberi
Metabolic Disorder | SpringerLink
Galactosemia, a Single Gene Disorder With Epigenetic Consequences | Pediatric Research
Screening for galactosemia: is there a place for it? | IJGM
PDF) Newborn Screening for Galactosemia in the United States: Looking Back, Looking Around, and Looking Ahead
What Is Galactosemia? — Galactosemia Foundation
The natural history of classic galactosemia: lessons from the GalNet registry | Orphanet Journal of Rare Diseases | Full Text
Developmental Outcomes in Duarte Galactosemia | Pediatrics | American Academy of Pediatrics
