Autosomal recessively inherited electrolyte excretory defect in the parotid of the “cribriform degeneration” mouse mutant — possible analogy to cystic fibrosis-Reference-Cited by-同舟云学术

Autosomal recessively inherited electrolyte excretory defect in the parotid of the “cribriform degeneration” mouse mutant — possible analogy to cystic fibrosis

Published:1974-08 Issue:4 Volume:15 Page:803-810
ISSN:0024-3205
Container-title:Life Sciences
language:en
Short-container-title:Life Sciences

Author:

Kaiser D.,Pivetta O.,Rennert O.M.

Publisher

Elsevier BV

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference9 articles.

1. Cribriform Degeneration ( cri ): A New Recessive Neurological Mutation in the Mouse

2. Secretion and transductal fluxes of ions in exocrine glands of the mouse

3. Excretion of the mono- and divalent ions in relation to flow rate in bartter's and pseudo bartter's syndromes in parotid saliva. comparative studies to the syndrome of conn

4. �ber passageres Harnkonzentrierungsverm�gen bei Fundulus heteroclitus

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