Loss of phosphatase activity in myotubularin-related protein 2 is associated with Charcot–Marie–Tooth disease type 4B1

By Berger P.  

Human Molecular Genetics, Vol. 11, Iss. 13, 2002-06 ,pp. : 1569-1579

Oxford University Press

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Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerve

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Human Molecular Genetics, Vol. 12, Iss. 14, 2003-07 ,pp. : 1713-1723

Oxford University Press

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Muscle-specific alternative splicing of myotubularin-related 1 gene is impaired in DM1 muscle cells

By Buj-Bello A.  

Human Molecular Genetics, Vol. 11, Iss. 19, 2002-07 ,pp. : 2297-2307

Oxford University Press

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Characterization of the myotubularin dual specificity phosphatase gene family from yeast to human

By Tentler D.  

Human Molecular Genetics, Vol. 7, Iss. 11, 1998-11 ,pp. : 1703-1712

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Elevation of insulin‐like growth factor binding protein‐2 level in Pallister–Killian syndrome: Implications for the postnatal growth retardation phenotype

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 6, 2015-06 ,pp. : 1268-1274

John Wiley & Sons Inc

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