Meeting Abstract 2024 · 0 atıf

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

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WoS Kategorileri

Biochemistry & Molecular Biology Genetics & Heredity

Künye

Dergi: EUROPEAN JOURNAL OF HUMAN GENETICS
Yıl: 2024
Cilt: 32
Sayfa: 1074-1074
ISSN: 1018-4813
eISSN: 1476-5438
WoS UID: WOS:001421430500753