Martin Krenn
0000-0003-3026-3082
3 papers found
Refreshing results…
Clinico‐genetic spectrum of limb‐girdle muscular weakness in Austria: A multicentre cohort study
Genotype‐guided diagnostic reassessment after exome sequencing in neuromuscular disorders: experiences with a two‐step approach
Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene
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