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Editorial

. 2018 Sep;22(5):737.

doi: 10.1016/j.ejpn.2018.07.010.

Genotype-phenotype correlation: The ultimate challenge in facioscapolohumeral muscular dystrophy

Rossella Tupler¹

Affiliations

Affiliation

¹ Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy; Department of Molecular Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, USA. Electronic address: rossella.tupler@unimore.it.

PMID: 30213505
DOI: 10.1016/j.ejpn.2018.07.010

Editorial

Genotype-phenotype correlation: The ultimate challenge in facioscapolohumeral muscular dystrophy

Rossella Tupler. Eur J Paediatr Neurol. 2018 Sep.

. 2018 Sep;22(5):737.

doi: 10.1016/j.ejpn.2018.07.010.

Author

Rossella Tupler¹

Affiliation

¹ Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy; Department of Molecular Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, USA. Electronic address: rossella.tupler@unimore.it.

PMID: 30213505
DOI: 10.1016/j.ejpn.2018.07.010

No abstract available

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Comment on

A 22-year follow-up reveals a variable disease severity in early-onset facioscapulohumeral dystrophy.
Goselink RJM, van Kernebeek CR, Mul K, Lemmers RJLF, van der Maarel SM, Brouwer OF, Voermans N, Padberg GW, Erasmus CE, van Engelen BGM. Goselink RJM, et al. Eur J Paediatr Neurol. 2018 Sep;22(5):782-785. doi: 10.1016/j.ejpn.2018.04.013. Epub 2018 May 3. Eur J Paediatr Neurol. 2018. PMID: 29753614

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