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LRRK2 Loss-of-Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact.
LRRK2 Loss-of-Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact.
2021
Christian Beetz
Ana Westenberger
Ruslan Al‐Ali
Najim Ameziane
Nadia Al-Hashmi
Rose-Mary Boustany
Fuad Al Mutairi
Majid Alfadhel
Zuhair N. Al-Hassnan
Moenaldeen AlSayed
Krishna Kumar Kandaswamy
Omid Paknia
Volha Skrahina
Arndt Rolfs
Peter Bauer
Keywords:
in patient
Loss function
Bioinformatics
Phenotype
MEDLINE
LRRK2
Medicine
Correction
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