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  2. Details for: Type I hyperprolinemia: genotype/phenotype correlations.
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Type I hyperprolinemia: genotype/phenotype correlations. [electronic resource]

By:
  • Guilmatre, Audrey
Contributor(s):
  • Legallic, Solenn
  • Steel, Gary
  • Willis, Alecia
  • Di Rosa, Gabriella
  • Goldenberg, Alice
  • Drouin-Garraud, Valérie
  • Guet, Agnès
  • Mignot, Cyril
  • Des Portes, Vincent
  • Valayannopoulos, Vassili
  • Van Maldergem, Lionel
  • Hoffman, Jodi D
  • Izzi, Claudia
  • Espil-Taris, Caroline
  • Orcesi, Simona
  • Bonafé, Luisa
  • Le Galloudec, Eric
  • Maurey, Hélène
  • Ioos, Christine
  • Afenjar, Alexandra
  • Blanchet, Patricia
  • Echenne, Bernard
  • Roubertie, Agathe
  • Frebourg, Thierry
  • Valle, David
  • Campion, Dominique
Producer: 20101020Description: 961-5 p. digitalISSN:
  • 1098-1004
Subject(s):
  • Adolescent
  • Adult
  • Alleles
  • Amino Acid Metabolism, Inborn Errors -- enzymology
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Female
  • Genetic Association Studies
  • Humans
  • Infant
  • Male
  • Mutation, Missense -- genetics
  • Proline -- metabolism
  • Proline Oxidase -- genetics
Online resources:
  • Available from publisher's website
In: Human mutation vol. 31
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Publication Type: Journal Article

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Type I hyperprolinemia: genotype/phenotype correlations.

APA

Guilmatre A., Legallic S., Steel G., Willis A., Di Rosa G., Goldenberg A., Drouin-Garraud V., Guet A., Mignot C., Des Portes V., Valayannopoulos V., Van Maldergem L., Hoffman J. D., Izzi C., Espil-Taris C., Orcesi S., Bonafé L., Le Galloudec E., Maurey H., Ioos C., Afenjar A., Blanchet P., Echenne B., Roubertie A., Frebourg T., Valle D. & Campion D. (20101020). Type I hyperprolinemia: genotype/phenotype correlations. : Human mutation.

Chicago

Guilmatre Audrey, Legallic Solenn, Steel Gary, Willis Alecia, Di Rosa Gabriella, Goldenberg Alice, Drouin-Garraud Valérie, Guet Agnès, Mignot Cyril, Des Portes Vincent, Valayannopoulos Vassili, Van Maldergem Lionel, Hoffman Jodi D, Izzi Claudia, Espil-Taris Caroline, Orcesi Simona, Bonafé Luisa, Le Galloudec Eric, Maurey Hélène, Ioos Christine, Afenjar Alexandra, Blanchet Patricia, Echenne Bernard, Roubertie Agathe, Frebourg Thierry, Valle David and Campion Dominique. 20101020. Type I hyperprolinemia: genotype/phenotype correlations. : Human mutation.

Harvard

Guilmatre A., Legallic S., Steel G., Willis A., Di Rosa G., Goldenberg A., Drouin-Garraud V., Guet A., Mignot C., Des Portes V., Valayannopoulos V., Van Maldergem L., Hoffman J. D., Izzi C., Espil-Taris C., Orcesi S., Bonafé L., Le Galloudec E., Maurey H., Ioos C., Afenjar A., Blanchet P., Echenne B., Roubertie A., Frebourg T., Valle D. and Campion D. (20101020). Type I hyperprolinemia: genotype/phenotype correlations. : Human mutation.

MLA

Guilmatre Audrey, Legallic Solenn, Steel Gary, Willis Alecia, Di Rosa Gabriella, Goldenberg Alice, Drouin-Garraud Valérie, Guet Agnès, Mignot Cyril, Des Portes Vincent, Valayannopoulos Vassili, Van Maldergem Lionel, Hoffman Jodi D, Izzi Claudia, Espil-Taris Caroline, Orcesi Simona, Bonafé Luisa, Le Galloudec Eric, Maurey Hélène, Ioos Christine, Afenjar Alexandra, Blanchet Patricia, Echenne Bernard, Roubertie Agathe, Frebourg Thierry, Valle David and Campion Dominique. Type I hyperprolinemia: genotype/phenotype correlations. : Human mutation. 20101020.

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