Author:
Yahalom Gilad,Anikster Yair,Huna-Baron Ruth,Hoffmann Chen,Blumkin Lubov,Lev Dorit,Tsabari Rakefet,Nitsan Zeev,Lerman Sheera F.,Ben-Zeev Bruria,Pode-Shakked Ben,Sofer Shira,Schweiger Avraham,Lerman-Sagie Tally,Hassin-Baer Sharon
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Reference25 articles.
1. Costeff H, Elpeleg O, Apter N, Divry P, Gadoth N (1993) 3-Methylglutaconic aciduria in “optic atrophy plus”. Ann Neurol 33:103–104
2. Elpeleg ON, Costeff H, Joseph A, Shental Y, Weitz R, Gibson KM (1994) 3-Methylglutaconic aciduria in the Iraqi-Jewish ‘optic atrophy plus’ (Costeff) syndrome. Dev Med Child Neurol 36(2):167–172
3. Costeff H, Gadoth N, Apter N, Prialnic M, Savir H (1989) A familial syndrome of infantile optic atrophy, movement disorder, and spastic paraplegia. Neurology 39:595–597
4. Zeharia A, Elpeleg ON, Mukamel M, Weitz R, Ariel R, Mimouni M (1992) 3-Methylglutaconic aciduria: a new variant. Pediatrics 89(6 Pt 1):1080–1082
5. Gonzalez IL (2005) Barth syndrome: tAZ gene mutations, mRNAs, and evolution. Am J Med Genet A 134(4):409–414
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