Novel Kmt2B Mutation Causes Cerebellar Ataxia: Expanding the Clinical Phenotype

AuthID
P-00V-BMZ
11
Author(s)
Santos, M
·
Samões, R
·
Araújo, M
·
Macedo, M
·
Sardoeira, A
·
Freitas, J
·
Tipo de Documento
Article
Year published
2021
Publicado
in Clinical Genetics, ISSN: 0009-9163
Volume: 100, Número: 6, Páginas: 743-747
Indexing
Publication Identifiers
SCOPUS: 2-s2.0-85114363891
Source Identifiers
ISSN: 0009-9163
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