A microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2)

Genomics

Volumn 49, Issue 1, 1998, Pages 143-146

  Matsumine, Hiroto ^a   Yamamura, Yasuhiro ^b   Hattori, Nobutaka ^a   Kobayashi, Tomonori ^a   Kitada, Tohru ^a   Yoritaka, Asako ^a   Mizuno, Yoshikuni ^a  

^a JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b HIROSHIMA UNIV SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; GENE DELETION; GENE LOCUS; HUMAN; INBREEDING; PARKINSONISM; PRIORITY JOURNAL; YEAST ARTIFICIAL CHROMOSOME;

EID: 0032054801     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.5196     Document Type: Article

References (8)

1. Ishikawa A., Tsuji S. Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism. Neurology. 47:1996;160-166.
2. Kruglyak L., Daly M. J., Reeve-Daly M. P., Lander E. S. Parametric and nonparametric linkage analysis: A unified multipoint approach. Am. J.Hum. Genet. 58:1996;1347-1363.
3. Lander S., Botstein D. Homozygosity mapping: A way to map human recessive traits with the DNA of inbred children. Science. 236:1987;1567-1570.
4. Matsumine H., Saito M., Matsubayashi S., Tanaka H., Ishikawa A., Hattori Y., Yokochi M., Kobayashi T., Igarashi S., Takano H., Sanpei K., Koike R., Mori H., Kondo T., Mizutani Y., Schaffer A. A., Yamamura Y., Nakamura S., Kuzuhara S., Tsuji S., Mizuno Y. Localization of a gene for an autosomal recessive form of juvenile parkinsonism to chromosome 6q25.2-27. Am. J. Hum. Genet. 60:1997;588-596.
5. Matsumine H., Yamamura Y., Kobayashi T., Nakamura S., Kuzuhara S., Mizuno Y. Early-onset parkinsonism with diurnal fluctuation maps to a locus for juvenile parkinsonism. Neurology. 1998.
6. Pappas G. J., Polymeropoulos M., Boyle J. M., Trent J. M. Regional assignment by hybrid mapping of 36 expressed sequence tags (ESTs) on human chromosome 6. Genomics. 25:1995;124-129.
7. Piontek K., Muller H. M., Fischer U., Gottert E., Batzer M. A., Meltzer P. S., Trent J. M., Meese E. Generation and characterization of a human chromosome 6-specific hncDNA library from a somatic cell hybrid. Cytogenet. Cell. Genet. 69:1995;273-278.
8. Yamamura Y., Sobue I., Ando K., Iida M., Yanagi T., Kono C. Paralysis agitance of early onset with marked diurnal fluctuation of symptoms. Neurology. 23:1973;239-244.