High incidence of spinal muscular atrophy type I (Werdnig ‐ Hoffmann disease) in the Karaite community in Israel

Clinical Genetics

Volumn 12, Issue 4, 1977, Pages 250-251

  Fried, K ^a   Mundel, G ^a  

^a TEL AVIV UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

DIAGNOSIS; ETIOLOGY; MAJOR CLINICAL STUDY; SPINAL MUSCULAR ATROPHY; WERDNIG HOFFMANN DISEASE;

CHILD, PRESCHOOL; CONSANGUINITY; FEMALE; GENE FREQUENCY; GENES, RECESSIVE; HUMAN; INFANT; ISRAEL; MALE; MUSCULAR ATROPHY; SPINAL CORD DISEASES;

EID: 0017662613     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1977.tb00934.x     Document Type: Article

References (4)

1. The nosology of the spinal muscular atrophies
2. Spinal muscular atrophy type II: a separate genetic and clinical entity from type I (Werdnig‐Hoffmann Disease) and type III (Kugelberg‐Welander Disease)
3. Some genetic polymorphic characters of the Karaite community