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Commentary: Galactosemia Diagnosis by Whole Exome Sequencing Later in Life

Friedman, J; Lucas-Del-Pozo, S; Moreno-Martinez, D; Camprodon-Gomez, M; Moreno-Martinez, D; Hernandez-Vara, J; Kurian, MA; (2021) Commentary: Galactosemia Diagnosis by Whole Exome Sequencing Later in Life. Movement Disorders Clinical Practice , 8 (S1) S40-S41. 10.1002/mdc3.13304. Green open access

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Type: Article
Title: Commentary: Galactosemia Diagnosis by Whole Exome Sequencing Later in Life
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1002/mdc3.13304
Publisher version: http://dx.doi.org/10.1002/mdc3.13304
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, Galactosemia, developmental delay, cerebral palsy
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Cancer Institute
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health > Developmental Neurosciences Dept
URI: https://discovery.ucl.ac.uk/id/eprint/10200074
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