Superficial siderosis: A potentially important cause of genetic as well as non-genetic deafness

American Journal of Medical Genetics

Volumn 130 A, Issue 1, 2004, Pages 22-25

  Dodson, Kelley M ^a,b   Sismanis, Aristides ^a   Nance, Walter E ^a  

^a VIRGINIA COMMONWEALTH UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

Author keywords

Alport syndrome; Cerebral cavernous malformation; Deafness; Genetics; Macrothrombocytopenia; MYH9; Superficial siderosis

Indexed keywords

FERRITIN; HEMOSIDERIN;

ATAXIA; BRAIN STEM; CENTRAL NERVOUS SYSTEM; CEREBELLUM; CONFERENCE PAPER; DEMYELINATION; GLIA; HEARING IMPAIRMENT; HUMAN; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SIDEROSIS; SPINAL CORD DISEASE; SUBARACHNOID HEMORRHAGE; SUPERFICIAL SIDEROSIS; VESTIBULOCOCHLEAR NERVE;

ATAXIA;

EID: 4344611147     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30050     Document Type: Conference Paper

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