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Publications by Gerald Hoefler
Aberrant Subcellular Localization of Peroxisomal 3-Ketoacyl-CoA Thiolase in the Zellweger Syndrome and Rhizomelic Chondrodysplasia Punctata
Pediatric Research
Child Health
Pediatrics
Perinatology
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118: Multiple Peroxisomal Enzyme Deficiencies in Rhizomelic Chondrodysplasia Punctata
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The Neurology of Rhizomelic Chondrodysplasia Punctata
Orphanet Journal of Rare Diseases
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Rhizomelic Chondrodysplasia Punctata: A Classic 'Spot' Diagnosis
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The 22-kD Peroxisomal Integral Membrane Protein in Zellweger Syndrome—Presence, Abundance, and Association With a Peroxisomal Thiolase Precursor Protein
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Rhizomelic Chondrodysplasia Punctata Type 1 Caused by a Novel Mutation in the PEX7 Gene
JCRPE Journal of Clinical Research in Pediatric Endocrinology
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Medical Journal Armed Forces India
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Lipidomics Analysis of Peroxisomal Disorders: Discovery of Deficits in Phosphatidyglycerol Levels in Rhizomelic Chondrodysplasia Type 1
Journal of Data Mining in Genomics & Proteomics
