Associated Papers
A New Intronic Variant in ECEL1 in Two Patients with Distal Arthrogryposis Type 5D.
Alesi V et al.
International Journal of Molecular Sciences, 2021
The Novel Compound Heterozygous Mutations of ECEL1 Identified in a Family with Distal Arthrogryposis Type 5D.
Jin JY et al.
Biomed Research International, 2020
The ECEL1-related strabismus phenotype is consistent with congenital cranial dysinnervation disorder.
Khan AO et al.
Journal of Aapos : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus, 2014
Mutations in ECEL1 cause distal arthrogryposis type 5D.
McMillin MJ et al.
American Journal of Human Genetics, 2013
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