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Journal of Movement Disorders
(Sep 2020)
A New Allelic Variant in the Gene in a Patient with Incomplete HARP Syndrome
Myriam Ley Martos,
María Jesús Salado Reyes,
Rosario Marín Iglesias,
Carmen Gutiérrez Moro,
Manuel Lubián Gutiérrez,
Lorena Estepa Pedregosa
Affiliations
Myriam Ley Martos
Department of Neuropediatrics, Puerta del Mar Hospital, Cádiz, Spain
María Jesús Salado Reyes
Department of Neuropediatrics, Puerta del Mar Hospital, Cádiz, Spain
Rosario Marín Iglesias
Department of Genetics, Puerta del Mar Hospital, Cádiz, Spain
Carmen Gutiérrez Moro
Department of Neuropediatrics, Puerta del Mar Hospital, Cádiz, Spain
Manuel Lubián Gutiérrez
Department of Neuropediatrics, Puerta del Mar Hospital, Cádiz, Spain
Lorena Estepa Pedregosa
Department of Critical Care, Puerta del Mar Hospital, Cádiz, Spain
DOI
https://doi.org/10.14802/jmd.19071
Journal volume & issue
Vol. 13, no. 3
pp. 229 – 231
Abstract
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No abstracts available.
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