Microcephaly, Short Stature, Intellectual Disability, Speech Absence and Cataract Are Associated with Novel Bi-Allelic Missense Variant in RTTN Gene: A Seckel Syndrome Case Report

Microcephaly, Short Stature, Intellectual Disability, Speech Absence and Cataract Are Associated with Novel Bi-Allelic Missense Variant in RTTN Gene: A Seckel Syndrome Case Report

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Veröffentlicht in:Children (Basel, Switzerland) Switzerland), 2023, Vol.10 (6)
Hauptverfasser: Mudassir, Behjat Ul, Agha, Zehra
Format: Report
Sprache:eng
Online-Zugang:Volltext
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ISSN:2227-9067
2227-9067
DOI:10.3390/children10061027