Distal arthrogryposis type 5D with novel clinical features and compound heterozygous mutations in ECEL1
Am J Med Genet A
.
2014 Jul;164A(7):1846-9.
doi: 10.1002/ajmg.a.36342.
Epub 2014 Apr 29.
Authors
Christopher P Barnett
1
,
Emily J Todd
,
Royston Ong
,
Mark R Davis
,
Vanessa Atkinson
,
Richard Allcock
,
Nigel Laing
,
Gianina Ravenscroft
Affiliation
1
Pediatric & Reproductive Genetics, SA Clinical Genetics Service, Women's and Children's Hospital/SA Pathology, North Adelaide, South Australia, Australia.
PMID:
24782201
DOI:
10.1002/ajmg.a.36342
No abstract available
Publication types
Case Reports
MeSH terms
Arthrogryposis / diagnosis*
Arthrogryposis / genetics*
Child, Preschool
Facies
Female
Heterozygote*
Humans
Metalloendopeptidases / genetics*
Mutation*
Phenotype*
Substances
ECEL1 protein, human
Metalloendopeptidases