Related references
Note: Only part of the references are listed.Connexin37 and Connexin43 deficiencies in mice disrupt lymphatic valve development and result in lymphatic disorders including lymphedema and chylothorax
John D. Kanady et al.
DEVELOPMENTAL BIOLOGY (2011)
Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype
Pia Ostergaard et al.
JOURNAL OF MEDICAL GENETICS (2011)
GJC2 Missense Mutations Cause Human Lymphedema
Robert E. Ferrell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
GJA1 Mutations, Variants, and Connexin 43 Dysfunction as it Relates to the Oculodentodigital Dysplasia Phenotype
William A. Paznekas et al.
HUMAN MUTATION (2009)
Estimating the population burden of lymphedema
Stanley G. Rockson et al.
LYMPHATIC CONTINUUM REVISITED (2008)
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia
AM Flenniken et al.
DEVELOPMENT (2005)
Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly
RR Richardson et al.
JOURNAL OF MEDICAL GENETICS (2004)
Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia
WA Paznekas et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)