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Molecular analysis of holocarboxylase synthetase deficiency: a missense mutation and a single base deletion are predominant in Japanese patients

✍ Scribed by Yoko Aoki; Yoichi Suzuki; Osamu Sakamoto; Xue Li; Kazutoshi Takahashi; Akira Ohtake; Ryoichi Sakuta; Toshihiro Ohura; Shigeaki Miyabayashi; Kuniaki Narisawa

Book ID: 116159951
Publisher: Elsevier Science
Year: 1995
Tongue: English
Weight: 777 KB
Volume: 1272
Category: Article
ISSN: 0925-4439
DOI: 10.1016/0925-4439(95)00082-8

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