Discover open access scientific publications

Search, annotate, share and cite publications

Publications by William D. Schall

Mutation Causing Von Willebrand’s Disease in Scottish Terriers

Journal of Veterinary Internal Medicine
MedicineVeterinary
2000English

Related publications

Investigating Autophagy Dysfunction Induced by a Parkinson's Disease-Causing Mutation in VPS35

English

NMNAT1 Mutation Causing Retinitis Pigmentosa

Acta Ophthalmologica
MedicineOphthalmology
2018English

A Disease Causing ATLASTIN 3 Mutation Affects Multiple Endoplasmic Reticulum-Related Pathways

Cellular and Molecular Life Sciences
Molecular NeuroscienceMolecular MedicineCell BiologyMolecular BiologyPharmacologyCellular
2019English

Novel Mutation in KCNQ2 Causing Ohtahara Syndrome

Annals of Child Neurology
2019English

Valvular Aortic Stenosis Causing Angiodysplasia and Acquired Von Willebrand's Disease: Heyde's Syndrome

BMJ Case Reports
Medicine
2014English

E148Q Is a Disease-Causing MEFV Mutation: A Phenotypic Evaluation in Patients With Familial Mediterranean Fever

Annals of the Rheumatic Diseases
ImmunologyMolecular BiologyBiochemistryRheumatologyAllergyGenetics
2005English

Novel CDHR1 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica
MedicineOphthalmology
2018English

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

Frontiers in Pediatrics
Child HealthPediatricsPerinatology
2017English

Novel C8ORF37 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica
MedicineOphthalmology
2018English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy