Work

Type 0 Spinal Muscular Atrophy Detected by Prenatal Exome Sequencing: Towards a Recognizable Fetal Phenotype

Year: 2026

Type: article

Abstract: Summary What's already known about this topic? What does this study add?

Source: Prenatal Diagnosis

DOI: 10.1002/pd.70041

Authors: M. Codina‐Solà, M. Costa‐Roger, A. Abulí, L. Blasco‐Pérez, D. Martínez‐Cruz, J. Leno‐Colorado, M. A. Sánchez‐Duran, S. Arévalo, N. Maiz, D. Gómez‐Andres, E. Vázquez, C. Rodó, E. F. Tizzano

Institutions: Vall d'Hebron Institut de Recerca, Vall d'Hebron Hospital Universitari

Language: English

Topic: Neurogenetic and Muscular Disorders Research

Subfield: Genetics

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

Funder: European Commission

Award: G434337789

OpenAlex ID: W7123777004

FWCI: 3.906

Cites: 11

Cited by: 1

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