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Publications by Ahmad H. Malli
Homozygosity for Non-H1069q Missense Mutations in ATP7B Gene and Early Severe Liver Disease: Report of Two Families and a Meta-Analysis
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Related publications
Fetuin-A and Fetuin-B in Non-Alcoholic Fatty Liver Disease: A Meta-Analysis and Meta-Regression
International Journal of Environmental Research and Public Health
Mutagenesis
Public Health
Environmental
Health
Toxicology
Occupational Health
Pollution
Two Novel Missense Substitutions in the VSX1 Gene: Clinical and Genetic Analysis of Families With Keratoconus From India
BMC Medical Genetics
Genetics
Apolipoprotein C3 Gene Polymorphisms Are Not a Risk Factor for Developing Non-Alcoholic Fatty Liver Disease: A Meta-Analysis
Hepatitis Monthly
Hepatology
Infectious Diseases
Identification of Novel Mutations and the Three Most Common Mutations in the Human ATP7B Gene of Korean Patients With Wilson Disease
Genetics in Medicine
Medicine
Genetics
Novel Missense Mutations in MYO7A Underlying Postlingual High- Or Low-Frequency Non-Syndromic Hearing Impairment in Two Large Families From China
Journal of Human Genetics
Genetics
Comparison of Severe and Non-Severe COVID-19 Pneumonia: Review and Meta-Analysis
Functional Characterization of Two Missense Mutations in Pex5p—C11S and N526K
Biochimica et Biophysica Acta - Molecular Cell Research
Cell Biology
Molecular Biology
Identification and Functional Analysis of Missense Mutations in the Lecithin Cholesterol Acyltransferase Gene in a Chilean Patient With Hypoalphalipoproteinemia
Lipids in Health and Disease
Biochemistry
Endocrinology
Clinical Biochemistry
Metabolism
Diabetes
Homozygosity for a FBN1 Missense Mutation: Clinical and Molecular Evidence for Recessive Marfan Syndrome
European Journal of Human Genetics
Genetics
