Results 141 to 150 of about 2,774 (188)

Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome. [PDF]

open access: yesAm J Hum Genet
Salpietro V   +66 more
europepmc   +1 more source

Case Report: autosomal dominant distal motor neuropathy as a new phenotype of <i>KIF21A</i>-related disorders. [PDF]

open access: yesFront Genet
Subbotin D   +7 more
europepmc   +1 more source

Finding the real COVID-19 case-fatality rates for SAARC countries

open access: yes, 2020
Tazir Shah MR   +4 more
europepmc   +1 more source

A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs). [PDF]

open access: yesAnn Neurol, 2019
Pareyson D   +41 more
europepmc   +1 more source

Modeling of Charcot-Marie-Tooth disease in zebrafish. [PDF]

open access: yesFront Mol Neurosci
Korzeniowska Née Wiweger M   +4 more
europepmc   +1 more source

LRRK2, gène majeur de la maladie de Parkinson dans les pays du Maghreb [PDF]

open access: yes, 2006
Brice, Alexis   +2 more
core   +1 more source

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