TY  - GEN
AU  - Weber,Stefanie
AU  - Schneider,Linda
AU  - Peters,Melanie
AU  - Misselwitz,Joachim
AU  - Rönnefarth,Gabriele
AU  - Böswald,Michael
AU  - Bonzel,Klaus E
AU  - Seeman,Tomas
AU  - Suláková,Tereza
AU  - Kuwertz-Bröking,Eberhard
AU  - Gregoric,Alojz
AU  - Palcoux,Jean-Bernard
AU  - Tasic,Velibor
AU  - Manz,Friedrich
AU  - Schärer,Karl
AU  - Seyberth,Hannsjörg W
AU  - Konrad,Martin
TI  - Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis
SN  - 1046-6673
PY  - 2001///1204
KW  - Adolescent
KW  - Amino Acid Sequence
KW  - genetics
KW  - Calcium
KW  - urine
KW  - Child
KW  - Child, Preschool
KW  - Claudins
KW  - Cohort Studies
KW  - Female
KW  - Genotype
KW  - Humans
KW  - Infant
KW  - Kidney
KW  - physiopathology
KW  - Magnesium
KW  - blood
KW  - Male
KW  - Membrane Proteins
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Nephrocalcinosis
KW  - Pedigree
KW  - Phenotype
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1681/ASN.V1291872
ER  -