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Publication
PropertyValue
Working Groups Klopstock
SubprojectNone
Open AccessOpen Access Yes
Publication TypeJournal Article
Peer ReviewedYes
PMIDPubMed ID 32707086
DOIDOI 10.1016/j.ajhg.2020.06.015
Publication Year2020
TitleBi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia. Wikidata
JournalAmerican journal of human genetics
ISSN0002-9297
ESSN1537-6605
URL https://www.ncbi.nlm.nih.gov/pubmed/?term=32707086%5Buid%5D
Pages364-373
Issue2
Volume107
Journal AbbreviationAm J Hum Genet
AuthorsHusain RA, Grimmel M, Wagner M, Hennings JC, Marx C, Feichtinger RG, Saadi A, Rostásy K, Radelfahr F, Bevot A, Döbler-Neumann M, Hartmann H, Colleaux L, Cordts I, Kobeleva X, Darvish H, Bakhtiari S, Kruer MC, Besse A, Ng AC, Chiang D, Bolduc F, Tafakhori A, Mane S, Ghasemi Firouzabadi S, Huebner AK, Buchert R, Beck-Woedl S, Müller AJ, Laugwitz L, Nägele T, Wang ZQ, Strom TM, Sturm M, Meitinger T, Klockgether T, Riess O, Klopstock T, Brandl U, Hübner CA, Deschauer M, Mayr JA, Bonnen PE, Krägeloh-Mann I, Wortmann SB, Haack TB
First AuthorHusain RA
Last AuthorHaack TB
ScholiaScholia Wikidata-based representation at Scholia

 External Resources

 Q97686537  Wikidata ID