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Details for article 79 of 588 found articles
| Title: |
EP.111Identification of novel biallelic mutations in SPTBN4 in a child with NEDHND featuring a spinal muscular atrophy phenotype |
| Author: |
Castiglioni, C. Kelly, R. Heather, M. Jofre, J. Suarez, B. Langley, W. Nagy, P. Fattori, F. Bertini, E. |
| Appeared in: |
Neuromuscular disorders |
| Paging: | Volume 29 (2019) nr. S1 pages S200 |
| Year: |
2019 |
| Contents: | |
| Publisher: |
Published by Elsevier B.V. |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 79 of 588 found articles
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