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Q41026907-7A908091-1B79-4DCC-9B08-197BB06C85DF
Q41026907-7A908091-1B79-4DCC-9B08-197BB06C85DF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41026907-7A908091-1B79-4DCC-9B08-197BB06C85DF
Confirmation that MAT1A p.Ala259Val mutation causes autosomal dominant hypermethioninemia.
P2860
Q41026907-7A908091-1B79-4DCC-9B08-197BB06C85DF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41026907-7A908091-1B79-4DCC-9B08-197BB06C85DF
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wasDerivedFrom
b3183cc109160ac881233b6c9c1616cbac946b2c
P2860
Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes.