Autosomal dominant ADAR c.3019G>A (p.(G1007R)) variant is an important mimic of hereditary spastic paraplegia and cerebral palsy-Reference-Cited by-同舟云学术

Autosomal dominant ADAR c.3019G>A (p.(G1007R)) variant is an important mimic of hereditary spastic paraplegia and cerebral palsy

Published:2022-02 Issue:2 Volume:44 Page:153-160
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Jones Hannah F.,Stoll Marion,Ho Gladys,O'Neill Dugald,Han Velda X.,Paget Simon,Stewart Kirsty,Lewis Jennifer,Kothur Kavitha,Troedson Christopher,Crow Yanick J.,Dale Russell C.,Mohammad Shekeeb S.

Funder

Research Foundation of Cerebral Palsy Alliance

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

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4. Janus kinase inhibition in the Aicardi-Goutieressyndrome;Vanderver;N Engl J Med,2020

5. Genetic, phenotypic, and interferon biomarker status in ADAR1-related neurological disease;Rice;Neuropediatrics,2017

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