APA

Hodes M. E., Zimmerman A. W., Aydanian A., Naidu S., Miller N. R., Garcia Oller J. L., Barker B., Aleck K. A., Hurley T. D. & Dlouhy S. R. (19990329). Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2). : American journal of medical genetics.

Chicago

Hodes M E, Zimmerman A W, Aydanian A, Naidu S, Miller N R, Garcia Oller J L, Barker B, Aleck K A, Hurley T D and Dlouhy S R. 19990329. Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2). : American journal of medical genetics.

Harvard

Hodes M. E., Zimmerman A. W., Aydanian A., Naidu S., Miller N. R., Garcia Oller J. L., Barker B., Aleck K. A., Hurley T. D. and Dlouhy S. R. (19990329). Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2). : American journal of medical genetics.

MLA

Hodes M E, Zimmerman A W, Aydanian A, Naidu S, Miller N R, Garcia Oller J L, Barker B, Aleck K A, Hurley T D and Dlouhy S R. Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2). : American journal of medical genetics. 19990329.