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

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Publication Details

Journal
Prenatal Diagnosis
Published
2026-01-13
DOI
https://doi.org/10.1002/pd.70041
Primary Topic
Neurogenetic and Muscular Disorders Research
Type
article
Field-Weighted Citation Impact
0.00

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article

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

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

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article en

Abstract

No abstract available for this paper.
Prenatal DiagnosisVol. 46(2)
Hebron University (PS), Vall d'Hebron Institut de Recerca (ES), Vall d'Hebron Hospital Universitari (ES)
European Commission
Zero hunger
Openalex Percentile: Top 89%
Neurogenetic and Muscular Disorders Research
DOIOpen Access PDFOpenAlex
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