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Publications by Jordan Fenner
Stomatocytosis and Spherocytosis in a Patient With Novel Heterozygous Novel Mutation in the Erythrocyte Protein 4.2 Gene and Parenteral Nutrition-Associated Liver Disease
Clinical Research and Trials
Related publications
A Novel Compound Heterozygous Mutation of the AIRE Gene in a Patient With Autoimmune Polyendocrine Syndrome Type 1
Annals of Pediatric Endocrinology and Metabolism
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
A Novel POLG Gene Mutation in a Patient With SANDO
Journal of Experimental and Integrative Medicine
Alternative Medicine
Complementary
Novel Hereditary Spherocytosis-Associated Splice Site Mutation in the ANK1 Gene Caused by Parental Gonosomal Mosaicism
Haematologica
Hematology
The Use of Omegaven in Treating Parenteral Nutrition-Associated Liver Disease
Journal of Perinatology
Gynecology
Child Health
Pediatrics
Perinatology
Obstetrics
Phytosterols Promote Liver Injury and Kupffer Cell Activation in Parenteral Nutrition-Associated Liver Disease
Science Translational Medicine
Medicine
Polyneuropathy in a Young Belgian Patient: A Novel Heterozygous Mutation in theWNK1/HSN2gene
Neurology: Genetics
Neurology
Genetics
A Novel Mutation of the Ceruloplasmin Gene in a Patient With Heteroallelic Ceruloplasmin Gene Mutation (HypoCPGM)
Tohoku Journal of Experimental Medicine
Biochemistry
Medicine
Genetics
Molecular Biology
Novel Prion Protein Gene Mutation in an Octogenarian With Creutzfeldt-Jakob Disease
Archives of Neurology
Novel KRIT1/CCM1 Heterozygous Nonsense Mutation (C.715 C>T) Associated With Cerebral and Cerebellar Cavernous Malformations in a Paediatric Patient
BMJ Case Reports
Medicine
