Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism (Q24320383)
scientific article published on 31 December 1993
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(P31) (Q13442814)
(P50) (Q88295024)
(P304) 1297-303
(P407) (Q1860)
(P433) 7
(P478) 75
(P577) Friday, December 31, 1993
(P921) (Q417801)
(Q14864210)
(Q1344835)
(Q1395332)
(Q1474877)
(P1433) (Q655814)
(P1476) "Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism" (language: en)
(P2093) M R Pollak
E M Brown
Y H Chou
S C Hebert
S J Marx
B Steinmann
T Levi
C E Seidman
(P2860) (Q67584191)
(Q27860612)
(Q41346416)
(Q41074853)
(Q25939003)
(Q28280066)
(Q29614810)
(Q34231539)
(Q70267498)
(Q43724437)
(Q28115244)
(Q71012104)
(Q37671598)
(Q33822121)
(Q34132473)
(Q69990581)
(Q70068222)
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description scientific article published on 31 December 1993

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