Cartilage-hair Hypoplasia Caused by Novel Compound Heterozygous RMRP Mutations.
Indian Pediatr
;
2011 July; 48(7): 559-561
Artigo
em Inglês
| 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.
Texto completo:
DisponíveL
Índice:
IMSEAR (Sudeste Asiático)
Idioma:
Inglês
Revista:
Indian Pediatr
Ano de publicação:
2011
Tipo de documento:
Artigo
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