KBP-cytoskeleton interactions underlie developmental anomalies in Goldberg-Shprintzen syndrome.
Drévillon, Loïc
KBP-cytoskeleton interactions underlie developmental anomalies in Goldberg-Shprintzen syndrome. [electronic resource] - Human molecular genetics Jun 2013 - 2387-99 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1460-2083
10.1093/hmg/ddt083 doi
Actins--genetics
Adolescent
Adult
Child
Craniofacial Abnormalities--genetics
Female
France
Hirschsprung Disease--genetics
Humans
Infant
Iraq
Male
Microtubules--genetics
Mutation
Nerve Tissue Proteins--genetics
Pedigree
Protein Binding
Tubulin--genetics
White People--genetics
KBP-cytoskeleton interactions underlie developmental anomalies in Goldberg-Shprintzen syndrome. [electronic resource] - Human molecular genetics Jun 2013 - 2387-99 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1460-2083
10.1093/hmg/ddt083 doi
Actins--genetics
Adolescent
Adult
Child
Craniofacial Abnormalities--genetics
Female
France
Hirschsprung Disease--genetics
Humans
Infant
Iraq
Male
Microtubules--genetics
Mutation
Nerve Tissue Proteins--genetics
Pedigree
Protein Binding
Tubulin--genetics
White People--genetics