Concepedia

Lein Dofash

LD

Statistics

Publications

3

Citations

55

H-Index

3

Active since

2022

Affiliations

The University of Western Australia(Current)

Hospital Universitario Virgen del Rocío

Harry Perkins Institute of Medical Research

Curtin University

UNSW Sydney

Lein Dofash is an author at The University of Western Australia specializing in molecular genetics, genetics, and medicine.

ORCID

Publications per year

2022–2024

3

Publications

3

A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry

Andrea Cortese, Sarah J. Beecroft, Stefano Facchini et al. · Nature Communications · 2024 · 28 citations · Full text

, , +17

Ablation of the carboxy-terminal end of <i>MAMDC2</i> causes a distinct muscular dystrophy

Fabiola Mavillard, Emilia Servián‐Morilla, Lein Dofash et al. · Brain · 2023 · 14 citations · Full text

, , +17

A <i>KLHL40</i> 3’ UTR splice-altering variant causes milder NEM8, an under-appreciated disease mechanism

Lein Dofash, Gavin Monahan, Emilia Servián‐Morilla et al. · Human Molecular Genetics · 2022 · 13 citations

, , +16

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