Genetic homogeneity between childhood-onset and adult-onset autosomal recessive spinal muscular atrophy

The Lancet

Volumn 346, Issue 8977, 1995, Pages 741-742

  Brahe, C ^a   Zappata, S ^a   Neri, G ^a   Servidei, S ^a   Ricci, E ^a   Tonali, P ^a  

^a CATHOLIC UNIVERSITY   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CLINICAL ARTICLE; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; FEMALE; GENE DELETION; HUMAN; HUMAN TISSUE; MALE; MOTONEURON; ONSET AGE; PRIORITY JOURNAL; SPINAL MUSCULAR ATROPHY;

EID: 0028978717     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(95)91507-9     Document Type: Article

References (5)

1. Classification of spinal muscular atrophies
2. The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy
3. Identification and characterization of a spinal muscular atrophy-determining gene
4. A clinical and genetic study of spinal muscular atrophy of adult onset
5. No evidence for linkage of autosomal dominant proximal spinal atrophies to chromosome 5q markers