Reply to: Double Trouble from POLG1 and CLCN1 Variants with Intrafamilial Phenotypic Heterogeneity

Martje G. Pauly; Sinem Tunc; Tobias Bäumer; Gabriele Gillessen-Kaesbach; Alexander Münchau

doi:10.1002/mdc3.12961

Reply to: Double Trouble from POLG1 and CLCN1 Variants with Intrafamilial Phenotypic Heterogeneity

Martje G. Pauly, Sinem Tunc, Tobias Bäumer, Gabriele Gillessen-Kaesbach, Alexander Münchau^*

^*Corresponding author for this work

Original language	English
Journal	Movement Disorders Clinical Practice
Volume	7
Issue number	5
Pages (from-to)	577-578
Number of pages	2
DOIs	https://doi.org/10.1002/mdc3.12961
Publication status	Published - 01.07.2020

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Research Area: Medical Genetics

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10.1002/mdc3.12961

Cite this

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author = "Pauly, {Martje G.} and Sinem Tunc and Tobias B{\"a}umer and Gabriele Gillessen-Kaesbach and Alexander M{\"u}nchau",

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AU - Tunc, Sinem

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AU - Gillessen-Kaesbach, Gabriele

AU - Münchau, Alexander

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M3 - Letters

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Reply to: Double Trouble from POLG1 and CLCN1 Variants with Intrafamilial Phenotypic Heterogeneity

Research Areas and Centers

UN SDGs

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