Cartilage-hair Hypoplasia Caused by Novel Compound Heterozygous RMRP Mutations.
Indian Pediatr
;
2011 July; 48(7): 559-561
Article
Dans Anglais
| IMSEAR
| ID: sea-168886
ABSTRACT
Cartilage-hair hypoplasia is a rare, autosomal recessive skeletal dysplasia, caused by mutations in the RMRP gene. The skeletal abnormalities include irregular metaphyses and cone shaped epiphyses of the hands. Molecular diagnosis confirmed two novel RMRP mutations in a compound heterozygous state in two siblings with this condition.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
langue:
Anglais
Texte intégral:
Indian Pediatr
Année:
2011
Type:
Article
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