A new rare mutation (691delCC/insAAA) in exon 17 of the PYGM gene causing McArdle disease

1. Quintans, B.
2. Sanchez-Andrade, A.
3. Teijeira, S.
4. Fernandez-Hojas, R.
5. Rivas, E.
6. López, M.J.
7. Navarro, C.

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DOI: 10.1001/ARCHNEUR.61.7.1108 GOOGLE SCHOLAR lock_openOpen access editor

Data source: Scopus