A Founder Mutation in CERKL Is a Major Cause of Retinal Dystrophy in Finland

Acta Ophthalmologica - United States
doi 10.1111/aos.13551
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Wiley

Related search

New POMT2 Mutations Causing Congenital Muscular Dystrophy: Identification of a Founder Mutation

Neurology
Neurology
2007English

Doyne Honeycomb Retinal Dystrophy/Malattia Leventinese Induced by EFEMP1 Mutation in a Chinese Family

BMC Ophthalmology
MedicineOphthalmology
2018English

Mutations in COL27A1 Cause Steel Syndrome and Suggest a Founder Mutation Effect in the Puerto Rican Population

European Journal of Human Genetics
Genetics
2014English

How Old Is This Mutation? - A Study of Three Ashkenazi Jewish Founder Mutations

BMC Genetics
Genetics
2010English

The p.P56S Mutation in theVAPBgene Is Not Due to a Single Founder: The First European Case

Clinical Genetics
Genetics
2010English

Corrections To: Source Confusion Is a Major Cause of Crowding

Journal of Vision
OphthalmologySensory Systems
2014English

Why Is High Persistence Alone a Major Cause of Concern?

Environmental Sciences: Processes and Impacts
ManagementMonitoringEnvironmentalPublic HealthMedicineEnvironmental ChemistryPolicyLawOccupational Health
2019English

Cytosine Deamination Is a Major Cause of Baseline Noise in Next-Generation Sequencing

Molecular Diagnosis and Therapy
MedicineMolecular MedicineGeneticsPharmacology
2014English

The Exon a (C77G) Mutation Is a Common Cause of Abnormal CD45 Splicing in Humans

Journal of Immunology
AllergyImmunology
2001English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy