Contribution to a book

DZNE-2020-00121

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Recessive ataxias

Synofzik, M. (First author)DZNE* ; Németh, A. H.

2018
Elsevier Amsterdam [u.a.]

This record in other databases:    

Please use a persistent id in citations: doi:10.1016/B978-0-444-64189-2.00005-6

Keyword(s): Ataxia: complications (MeSH) ; Ataxia: genetics (MeSH) ; Cytoskeletal Proteins (MeSH) ; Genes, Recessive: genetics (MeSH) ; Heredodegenerative Disorders, Nervous System: diagnostic imaging (MeSH) ; Heredodegenerative Disorders, Nervous System: genetics (MeSH) ; Humans (MeSH) ; Molecular Diagnostic Techniques (MeSH) ; Mutation: genetics (MeSH) ; Nerve Tissue Proteins: genetics (MeSH) ; Neuroimaging (MeSH) ; Nuclear Proteins: genetics (MeSH) ; Spinocerebellar Ataxias: classification (MeSH) ; Spinocerebellar Ataxias: diagnostic imaging (MeSH) ; Spinocerebellar Ataxias: genetics (MeSH) ; Vitamin E Deficiency: complications (MeSH) ; Vitamin E Deficiency: genetics (MeSH)

---

Contributing Institute(s):

1. Parkinson Genetics (AG Gasser 1)

Research Program(s):

1. 345 - Population Studies and Genetics (POF3-345) (POF3-345)

Appears in the scientific report 2018

---

Database coverage:
; NCBI Molecular Biology Database ; SCOPUS

---