A family with X-linked creatine transporter deficiency diagnosed by whole exome sequencing
Publication
, Conference
Mori, M; Goldstein, JL; Young, SP; Millington, DS; Koeberl, DD
Published in: MOLECULAR GENETICS AND METABOLISM
March 1, 2015
Duke Scholars
Published In
MOLECULAR GENETICS AND METABOLISM
EISSN
1096-7206
ISSN
1096-7192
Publication Date
March 1, 2015
Volume
114
Issue
3
Start / End Page
344 / 345
Location
Salt Lake City, UT
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Conference Name
38th Annual Meeting of the Society-for-Inherited-Metabolic-Disorders (SIMD)
Related Subject Headings
- Genetics & Heredity
- 3202 Clinical sciences
- 3105 Genetics
- 1103 Clinical Sciences
Citation
APA
Chicago
ICMJE
MLA
NLM
Mori, M., Goldstein, J. L., Young, S. P., Millington, D. S., & Koeberl, D. D. (2015). A family with X-linked creatine transporter deficiency diagnosed by whole exome sequencing. In MOLECULAR GENETICS AND METABOLISM (Vol. 114, pp. 344–345). Salt Lake City, UT: ACADEMIC PRESS INC ELSEVIER SCIENCE.
Mori, Mad, Jennifer L. Goldstein, Sarah P. Young, David S. Millington, and Dwight D. Koeberl. “A family with X-linked creatine transporter deficiency diagnosed by whole exome sequencing.” In MOLECULAR GENETICS AND METABOLISM, 114:344–45. ACADEMIC PRESS INC ELSEVIER SCIENCE, 2015.
Mori M, Goldstein JL, Young SP, Millington DS, Koeberl DD. A family with X-linked creatine transporter deficiency diagnosed by whole exome sequencing. In: MOLECULAR GENETICS AND METABOLISM. ACADEMIC PRESS INC ELSEVIER SCIENCE; 2015. p. 344–5.
Mori, Mad, et al. “A family with X-linked creatine transporter deficiency diagnosed by whole exome sequencing.” MOLECULAR GENETICS AND METABOLISM, vol. 114, no. 3, ACADEMIC PRESS INC ELSEVIER SCIENCE, 2015, pp. 344–45.
Mori M, Goldstein JL, Young SP, Millington DS, Koeberl DD. A family with X-linked creatine transporter deficiency diagnosed by whole exome sequencing. MOLECULAR GENETICS AND METABOLISM. ACADEMIC PRESS INC ELSEVIER SCIENCE; 2015. p. 344–345.
Published In
MOLECULAR GENETICS AND METABOLISM
EISSN
1096-7206
ISSN
1096-7192
Publication Date
March 1, 2015
Volume
114
Issue
3
Start / End Page
344 / 345
Location
Salt Lake City, UT
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Conference Name
38th Annual Meeting of the Society-for-Inherited-Metabolic-Disorders (SIMD)
Related Subject Headings
- Genetics & Heredity
- 3202 Clinical sciences
- 3105 Genetics
- 1103 Clinical Sciences