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
·
Document Type
Article
Year published
2021
Published
in Clinical Genetics, ISSN: 0009-9163
Volume: 100, Issue: 6, Pages: 743-747
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Publication Identifiers
SCOPUS: 2-s2.0-85114363891
Source Identifiers
ISSN: 0009-9163
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