宗像可枝 (Kae Munakata) - マイポータル

基本情報

Mitochondrial DNA mutation 3644T→C associated with bipolar disorder.

Genomics 84(6) 1041-1050 2004年12月
Mitochondrial DNA 3644T -> C mutation associated with bipolar disorder

K Munakata, M Tanaka, K Mori, S Washizuka, M Yoneda, O Tajima, T Akiyama, S Nanko, H Kunugi, K Tadokoro …

GENOMICS 84(6) 1041-1050 2004年12月
Clinical implications of duplicated mtDNA in Pearson syndrome

K Muraki, N Sakura, H Ueda, H Kihara, Y Goto

AMERICAN JOURNAL OF MEDICAL GENETICS 98(3) 205-209 2001年1月
Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene

J Akanuma, K Muraki, H Komaki, Nonaka, I, Y Goto

JOURNAL OF HUMAN GENETICS 45(6) 337-341 2000年
Pearson症候群の臨床像と分子遺伝学的検討

村木可枝

日本小児血液学会誌 13(5) 346-352 1999年
Clinical Features and Molecular Genetic Study of Pearson syndrome.

Kae MURAKI

Japanese Journal of Pediatric Hematology 13(5) 346-352 1999年
The association between haematological manifestation and mtDNA deletions in Pearson syndrome

K Muraki, S Nishimura, Y Goto, Nonaka, I, N Sakura, K Ueda

JOURNAL OF INHERITED METABOLIC DISEASE 20(5) 697-703 1997年9月
Severe lactic acidosis and neonatal death in Pearson syndrome

K Muraki, Y Goto, Nishino, I, M Hayashidani, S Takeuchi, S Horai, N Sakura, K Ueda

JOURNAL OF INHERITED METABOLIC DISEASE 20(1) 43-48 1997年3月