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- NP708211.RABKLJZUv0EPhQL6kQ9F42JfA9KDtYOcB7o5Hrsm-Qwh4130_assertion type Assertion NP708211.RABKLJZUv0EPhQL6kQ9F42JfA9KDtYOcB7o5Hrsm-Qwh4130_head.
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- NP708211.RABKLJZUv0EPhQL6kQ9F42JfA9KDtYOcB7o5Hrsm-Qwh4130_assertion SIO_000772 19068277 NP708211.RABKLJZUv0EPhQL6kQ9F42JfA9KDtYOcB7o5Hrsm-Qwh4130_provenance.
- NP708211.RABKLJZUv0EPhQL6kQ9F42JfA9KDtYOcB7o5Hrsm-Qwh4130_assertion evidence source_evidence_literature NP708211.RABKLJZUv0EPhQL6kQ9F42JfA9KDtYOcB7o5Hrsm-Qwh4130_provenance.
- NP708211.RABKLJZUv0EPhQL6kQ9F42JfA9KDtYOcB7o5Hrsm-Qwh4130_assertion description "[Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708211.RABKLJZUv0EPhQL6kQ9F42JfA9KDtYOcB7o5Hrsm-Qwh4130_provenance.