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Meeting Abstract 2024 · 0 citations

A case of Perrault syndrome with a novel variant diagnosed at a late stage with predominance of neurological findings

Kina, Hacer Ukba, Cinkara, Neslihan, Kanjee, Momen

Abstract

No abstract available for this publication.

WoS Categories
Biochemistry & Molecular Biology Genetics & Heredity
Citation
Journal
EUROPEAN JOURNAL OF HUMAN GENETICS
Year
2024
Volume
32
Pages
1074-1074
ISSN
1018-4813
eISSN
1476-5438
WoS UID
WOS:001421430500753