about
Long-distance communication by specialized cellular projections during pigment pattern development and evolution.Abnormal glycosylation in Joubert syndrome type 10.Interpreting the clinical significance of combined variants in multiple recessive disease genes: systematic investigation of Joubert syndrome yields little support for oligogenicity.Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish.Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction.Rhombencephalosynapsis: Fused cerebellum, confused geneticists.MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon Guidance
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Q36610004-4A2AC5FB-1969-4E61-8185-D9327F68DED5Q37719527-A6FF00F9-007D-429A-8232-78176954DC08Q38644622-6E0DF53B-8131-4CC0-8764-A7DAC8E75D7FQ38669720-17D86674-9FEF-46B1-AF13-15308421F788Q41918892-DC12AD65-81A6-403F-A8EA-140E80919816Q64958348-FF9BC443-D84C-4A6E-B8C8-7DE982613948Q93341697-359B3C80-7847-4C3F-A26D-D786529F841F
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Megan E Grout
@en
Megan E Grout
@nl
type
label
Megan E Grout
@en
Megan E Grout
@nl
prefLabel
Megan E Grout
@en
Megan E Grout
@nl
P31
P496
0000-0001-7704-2100