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Publications by Anil K. Mandal
Disease-Causing Mutations in Proteins: Structural Analysis of the CYP1b1 Mutations Causing Primary Congenital Glaucoma in Humans
Biophysical Journal
Biophysics
Globally,CYP1B1Mutations in Primary Congenital Glaucoma Are Strongly Structured by Geographic and Haplotype Backgrounds
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
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The Structural Context of Disease-Causing Mutations in Gap Junctions
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
A Spectrum of CYP1B1 Mutations Associated With Primary Congenital Glaucoma in Families of Pakistani Descent
Human Genome Variation
Biochemistry
Genetics
Molecular Biology
ENU Induced Mutations Causing Congenital Cardiovascular Anomalies
Development (Cambridge)
Developmental Biology
Molecular Biology
Structural and Functional Consequences of Mutations in 6-Pyruvoyltetrahydropterin Synthase Causing Hyperphenylalaninemia in Humans
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Disease-Causing Mutations in Genes of the Complement System
American Journal of Human Genetics
Genetics
Mutations in CYP1B1, the Gene for Cytochrome P4501B1, Are the Predominant Cause of Primary Congenital Glaucoma in Saudi Arabia
American Journal of Human Genetics
Genetics
CYP1B1 Mutations in French Patients With Early-Onset Primary Open-Angle Glaucoma
Journal of Medical Genetics
Genetics
Disease-Causing Missense Mutations in Human DNA Helicase Disorders
Mutation Research - Reviews in Mutation Research
Mutagenesis
Health
Genetics
Toxicology
Mutations in LAMB2 Causing a Severe Form of Synaptic Congenital Myasthenic Syndrome
Journal of Medical Genetics
Genetics