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Journal description
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Details for article 102 of 451 found articles
| Title: |
Congenital fiber type disproportion myopathy and novel compound heterozygous mutations in the RYR1 gene. Next generation sequencing – A first line diagnostic tool for congenital myopathy |
| Author: |
Takamura, K. Dalton, J. Karachunski, P. |
| Appeared in: |
Neuromuscular disorders |
| Paging: | Volume 26 (2016) nr. S2 pages 1 p. |
| Year: |
2016 |
| Contents: | |
| Publisher: |
Published by Elsevier B.V. |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 102 of 451 found articles
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