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Publications by Cathryn S Mellersh

A Novel Mutation in TTC8 Is Associated With Progressive Retinal Atrophy in the Golden Retriever

Canine Genetics and Epidemiology

English

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A Novel Mutation (LEU396ARG) in OPA1 Is Associated With a Severe Phenotype in a Large Dominant Optic Atrophy Pedigree

Sensory Systems

English

Correction: APOE Ε4 Is Associated With Disproportionate Progressive Hippocampal Atrophy in AD

Multidisciplinary

English

A Novel Mutation in CELSR1 Is Associated With Hereditary Lymphedema

Computer Networks

Developmental Neuroscience

English

A Novel Missense Mutation in USP26 Gene Is Associated With Nonobstructive Azoospermia

Reproductive Sciences

English

A Patient With Posterior Cortical Atrophy Possesses a Novel Mutation in the Presenilin 1 Gene

Multidisciplinary

English

Progressive Muscle Atrophy With Hypokalaemic Periodic Paralysis and Calcium Channel Mutation

Aktuelle Neurologie

English

A Novel KAL1 Mutation Is Associated With Combined Pituitary Hormone Deficiency

Human Genome Variation

Molecular Biology

English

A Novel ROGDI Gene Mutation Is Associated With Kohlschutter-Tonz Syndrome

Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology

Nuclear Medicine

Forensic Medicine

English

Impairment of Mitochondrial tRNAIle Processing by a Novel Mutation Associated With Chronic Progressive External Ophthalmoplegia

Molecular Medicine

Molecular Biology

English