Spinal muscle atrophy type 1 (Werdnig-Hoffman disease) with complex cardiac malformation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00431-004-1437-6.pdf
Reference8 articles.
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2. Devriendt K, Lammens M, Schollen E, Van Hole C, Dom R, Devlieger H (1996) Clinical and molecular genetic features of congenital spinal muscle atrophy. Ann Neurol 40: 731–738
3. Finsterer J, Sollberger C (1999) Cardiac involvement in Werdnig-Hoffmann’s spinal muscle atrophy. Cardiology 92: 178–182
4. Moller P, Saugstad OD, Skullerud K, Velken M, Berg K, Nitter-Hauge S (1990) Spinal muscle atrophy type I combined with atrial septal defect in three sibs. Clin Genet 38: 81–83
5. Mulleners WM, van Ravenswaay CM, Gabreels FJM, Hamel BC, van Oort A, Sengers RCA (1996) Spinal muscle atrophy combined with congenital heart disease: a report of two cases. Neuropediatrics 27: 333–334
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