Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism (Q24320383)

From Wikidata
Jump to navigation Jump to search
scientific article published on 31 December 1993
edit
Language Label Description Also known as
English
Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
scientific article published on 31 December 1993

    Statements

    Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism (English)
    0 references
    M R Pollak
    0 references
    E M Brown
    0 references
    Y H Chou
    0 references
    S C Hebert
    0 references
    S J Marx
    0 references
    B Steinmann
    0 references
    T Levi
    0 references
    C E Seidman
    0 references
    31 December 1993
    0 references
    0 references
    75
    0 references
    7
    0 references
    1297-303
    0 references

    Identifiers

     
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    edit