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Atypical methylmalonic aciduria with progressive encephalopathy, microcephaly and cataract in two siblings — a new recessive syndrome?

✍ Scribed by P. Strómme; O. Stokke; E. Jellum; O.K. Skjeldal; R. Baumgartner


Book ID
115091689
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
604 KB
Volume
48
Category
Article
ISSN
0009-9163

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