Conference
A 9 nt deletion in mt DNA in 2 siblings with pervasive developmental disorder (PDD) and mitochondrial myopathy.
Authors
Rupar CA; Gordon BA; Kronick JB; Levin SD; Ramsay DA; Fox M; Szatmari P
Volume
61
Pagination
pp. A319-A319
Publisher
CELL PRESS
Publication Date
October 1, 1997
Conference proceedings
AMERICAN JOURNAL OF HUMAN GENETICS
Issue
4
ISSN
0002-9297