Title not supplied

Brusilow

1995

Structure and expression of a complementary DNA for the nuclear coded precursor of human mitochondrial ornithine transcarbamylase.

Horwich AL, Fenton WA, Williams KR, Kalousek F, Kraus JP, Doolittle RF, Konigsberg W, Rosenberg LE

Science, (4653):1068-1074 1984

MED: 6372096

Structure of the human ornithine transcarbamylase gene.

Hata A, Tsuzuki T, Shimada K, Takiguchi M, Mori M, Matsuda I

J Biochem, (2):302-308 1988

MED: 2836378

Estimated frequency of urea cycle enzymopathies in Japan.

Nagata N, Matsuda I, Oyanagi K

Am J Med Genet, (2):228-229 1991

MED: 2063931

Human gene therapy comes of age.

Miller AD

Nature, (6378):455-460 1992

MED: 1608446

Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies.

Msall M, Batshaw ML, Suss R, Brusilow SW, Mellits ED

N Engl J Med, (23):1500-1505 1984

MED: 6717540

Retrospective survey of urea cycle disorders: Part 2. Neurological outcome in forty-nine Japanese patients with urea cycle enzymopathies.

Nagata N, Matsuda I, Matsuura T, Oyanagi K, Tada K, Narisawa K, Kitagawa T, Sakiyama T, Yamashita F, Yoshino M

Am J Med Genet, (4):477-481 1991

MED: 1746614

Late-onset ornithine transcarbamylase deficiency in male patients.

Finkelstein JE, Hauser ER, Leonard CO, Brusilow SW

J Pediatr, (6):897-902 1990

MED: 2246687

Retrospective survey of urea cycle disorders: Part 1. Clinical and laboratory observations of thirty-two Japanese male patients with ornithine transcarbamylase deficiency.

Matsuda I, Nagata N, Matsuura T, Oyanagi K, Tada K, Narisawa K, Kitagawa T, Sakiyama T, Yamashita F, Yoshino M

Am J Med Genet, (1):85-89 1991

MED: 2012137

Biochemical heterogeneity of ornithine carbamoyl transferase(OCT) in patients with OCT deficiency.

Matsuda I, Nagata N, Ohyanagi K, Tsuchiyama A, Yamamoto H, Hase Y, Kodama H, Kai Y

Jinrui Idengaku Zasshi, (3):327-333 1984

MED: 6442743