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Publications by Liina Kuuluvainen

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

Acta Ophthalmologica

English

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

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

BMC Ophthalmology

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

European Journal of Human Genetics

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

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

Clinical Genetics

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Corrections To: Source Confusion Is a Major Cause of Crowding

Journal of Vision

Sensory Systems

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Why Is High Persistence Alone a Major Cause of Concern?

Environmental Sciences: Processes and Impacts

Environmental Chemistry

Occupational Health

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

Molecular Diagnosis and Therapy

Molecular Medicine

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

Journal of Immunology

English