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authFullName_s : Muhammad Umair
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A Homozygous Missense Variant in PPP1R1B/DARPP‐32 Is Associated With Generalized Complex Dystonia

Amjad Khan , Anne Molitor , Sylvain Mayeur , Gaoqun Zhang , Bruno Rinaldi et al.
Movement Disorders, 2022, 37 (2), pp.365-374. ⟨10.1002/mds.28861⟩
Journal articles hal-03509022v1

Variants in the PNPLA1 Gene in Families with Autosomal Recessive Congenital Ichthyosis Reveal Clinical Significance

Farooq Ahmad , Ishtiaq Ahmed , Qamre Alam , Tanveer Ahmad , Ammara Khan et al.
Molecular Syndromology, 2021, 12 (6), pp.351-361. ⟨10.1159/000516943⟩
Journal articles hal-03948042v1
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Developing a Laser Induced Liquid Beam Ion Desorption Spectral Database as Reference for Spaceborne Mass Spectrometers

Fabian Klenner , Muhammad Umair , Sebastian Walter , Nozair Khawaja , Jon Hillier et al.
Earth and Space Science, 2022, ⟨10.1029/2022EA002313⟩
Journal articles insu-03774741v1