Diagnostic strategy for inherited hypomagnesemia.

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Diagnostic strategy for inherited hypomagnesemia.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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Diagnostic strategy for inherited hypomagnesemia.

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Diagnostic strategy for inherited hypomagnesemia.

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Diagnostic strategy for inherited hypomagnesemia.

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Diagnostic strategy for inherited hypomagnesemia.

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Diagnostic strategy for inherited hypomagnesemia.

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Diagnostic strategy for inherited hypomagnesemia.

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P1476

Diagnostic strategy for inherited hypomagnesemia.

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P2093

Hiroko Togawa

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Hiroshi Kaito

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Ichiro Morioka

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Junya Fujimura

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Kandai Nozu

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Kazumoto Iijima

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Keita Nakanishi

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Koichi Kamei

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Koichi Nakanishi

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Naohiro Kamiyoshi

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P2860

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption

CNNM2, encoding a basolateral protein required for renal Mg2+ handling, is mutated in dominant hypomagnesemia

A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement

Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

Epithelial inflammation resulting from an inherited loss-of-function mutation in EGFR

P2888

s10157-017-1396-7

P304

1003-1010

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P31

scholarly article

P356

10.1007/S10157-017-1396-7

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P433

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P478

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P50

Tomohiko Yamamura

Shogo Minamikawa

P577

2017-03-01T00:00:00Z

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P698

28251383

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