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Q42752422-C9D95C59-F03C-4B70-98F6-F2F3B81F49E5
Q42752422-C9D95C59-F03C-4B70-98F6-F2F3B81F49E5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752422-C9D95C59-F03C-4B70-98F6-F2F3B81F49E5
Loss of ALDH18A1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3A and Warburg Micro syndrome.
P2860
Q42752422-C9D95C59-F03C-4B70-98F6-F2F3B81F49E5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42752422-C9D95C59-F03C-4B70-98F6-F2F3B81F49E5
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wasDerivedFrom
0bdc4117b652c4ccdc60afa0d1bc32ab225e73c2
P2860
Understanding pyrroline-5-carboxylate synthetase deficiency: clinical, molecular, functional, and expression studies, structure-based analysis, and novel therapy with arginine