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GNE gene

Discuss publications and research concerning the GNE gene.

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Related literature

GNE Mutation-related Congenital Thrombocytopenia in 2 Siblings: Case Reports and Literature Review.
GNE
Hydroxyethylamine & phthalimide analogs restoring defects due to GNE dysfunction: rare disease therapeutic significance.
GNE
Mutation in GNE is associated with severe congenital thrombocytopenia.
GNE
GNE myopathy caused by a synonymous mutation leading to aberrant mRNA splicing.
GNE
GNE myopathy in a Chinese male with a novel homozygous mutation.
GNE
Skeletal Muscle in Healthy Subjects versus Those with GNE-Related Myopathy: Evaluation with Shear-Wave US--A Pilot Study.
GNE
Mutational spectrum and clinical features in 35 unrelated mainland Chinese patients with GNE myopathy.
GNE
Muscle biopsy and UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene mutation analysis in two Chinese patients with distal myopathy with rimmed vacuoles.
GNE
GNE myopathy associated with congenital thrombocytopenia: a report of two siblings.
GNE
Gne depletion during zebrafish development impairs skeletal muscle structure and function.
GNE

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