Novel Mechanism of Cerebral Folate Deficiency with Compound Heterozygous Variants in Reduced Folate Carrier (SLC19A1) in Two Siblings Manifesting with Acute Brainstem Lesions (Atypical ADEM) (P8-6.006)

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Journal
Neurology
Published
2025-04-07
DOI
https://doi.org/10.1212/wnl.0000000000211443
Primary Topic
Folate and B Vitamins Research
Type
article
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article

Novel Mechanism of Cerebral Folate Deficiency with Compound Heterozygous Variants in Reduced Folate Carrier (SLC19A1) in Two Siblings Manifesting with Acute Brainstem Lesions (Atypical ADEM) (P8-6.006)

Ai Sakonju, Sanjit Sah
Neurology
Folate and B Vitamins Research
article

Novel Mechanism of Cerebral Folate Deficiency with Compound Heterozygous Variants in Reduced Folate Carrier (SLC19A1) in Two Siblings Manifesting with Acute Brainstem Lesions (Atypical ADEM) (P8-6.006)

Ai Sakonju, Sanjit Sah
article en

Abstract

No abstract available for this paper.
NeurologyVol. 104(7_Supplement_1)
SUNY Upstate Medical University (US)
Zero hunger
Openalex Percentile: Top 89%
Folate and B Vitamins Research
DOISourceOpenAlex
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Novel Mechanism of Cerebral Folate Deficiency with Compound Heterozygous Variants in Reduced Folate Carrier (SLC19A1) in Two Siblings Manifesting with Acute Brainstem Lesions (Atypical ADEM) (P8-6.006) — Ai Sakonju, Sanjit Sah · Neurology (2025) | TGRS Research Map | TGRS