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11 results on '"Hsu JH"'

2. Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2.

Author

Niu DM, Lin HY, Wu TJ, Hsu JH, Yu HC, Lin SP, Chuang CK, and Huang CH

Subjects
Amino Acid Substitution, Base Sequence, Codon genetics, Glycogen Storage Disease Type II enzymology, Humans, Leukocytes, Mononuclear enzymology, Mutation, Missense, alpha-Glucosidases blood, alpha-Glucosidases deficiency, Glycogen Storage Disease Type II genetics, alpha-Glucosidases genetics
Published
2010

3. Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2.

Author

Niu DM, Lin HY, Wu TJ, Hsu JH, Yu HC, Lin SP, Chuang CK, and Huang CH

Subjects
Amino Acid Substitution, Base Sequence, Codon genetics, Glycogen Storage Disease Type II enzymology, Humans, Leukocytes, Mononuclear enzymology, Mutation, Missense, alpha-Glucosidases blood, alpha-Glucosidases deficiency, Glycogen Storage Disease Type II genetics, alpha-Glucosidases genetics
Published
2010

4. Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2.

Author

Niu DM, Lin HY, Wu TJ, Hsu JH, Yu HC, Lin SP, Chuang CK, and Huang CH

Subjects
Amino Acid Substitution, Base Sequence, Codon genetics, Glycogen Storage Disease Type II enzymology, Humans, Leukocytes, Mononuclear enzymology, Mutation, Missense, alpha-Glucosidases blood, alpha-Glucosidases deficiency, Glycogen Storage Disease Type II genetics, alpha-Glucosidases genetics
Published
2010

6. Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2.

Author

Lin HY, Wu TJ, Hsu JH, Yu HC, Lin SP, Chuang CK, Huang CH, and Niu DM

Subjects
Amino Acid Substitution, Base Sequence, Codon genetics, Glycogen Storage Disease Type II enzymology, Humans, Leukocytes, Mononuclear enzymology, Mutation, Missense, alpha-Glucosidases blood, alpha-Glucosidases deficiency, Glycogen Storage Disease Type II genetics, alpha-Glucosidases genetics
Published
2010

7. Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2.

Author

Lin HY, Wu JT, Hsu JH, Yu HC, Lin SP, Huang CH, and Niu DM

Subjects
Amino Acid Substitution, Base Sequence, Codon genetics, Glycogen Storage Disease Type II enzymology, Humans, Leukocytes, Mononuclear enzymology, Mutation, Missense, alpha-Glucosidases blood, alpha-Glucosidases deficiency, Glycogen Storage Disease Type II genetics, alpha-Glucosidases genetics
Published
2010

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