Homozygous SMN1 exons 1–6 deletion: Pitfalls in genetic...

American Journal of Medical Genetics Part A 2012 Vol. 158A; Iss. 7

Homozygous SMN1 exons 1–6 deletion: Pitfalls in genetic counseling and general recommendations for spinal muscular atrophy molecular diagnosis

C. Thauvin-Robinet, S. Drunat, P. Saugier Veber, D. Chantereau, M. Cossée, C. Cassini, P. Soichot, A. Masurel-Paulet, J.V. De Monléon, P. Sagot, F. Huet, M. Antin, N. Calmels, L. Faivre, B. Gérard, le
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Volume:
158A
Year:
2012
Language:
english
Pages:
1
DOI:
10.1002/ajmg.a.35402
File:
PDF, 297 KB
english, 2012
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