Familial hypomagnesaemia with secondary hypocalcaemia.

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Familial hypomagnesaemia with secondary hypocalcaemia.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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name

Familial hypomagnesaemia with secondary hypocalcaemia.

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Familial hypomagnesaemia with secondary hypocalcaemia.

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type

Item

label

Familial hypomagnesaemia with secondary hypocalcaemia.

@en

Familial hypomagnesaemia with secondary hypocalcaemia.

@nl

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Familial hypomagnesaemia with secondary hypocalcaemia.

@en

Familial hypomagnesaemia with secondary hypocalcaemia.

@nl

P1476

Familial hypomagnesaemia with secondary hypocalcaemia.

@en

P2093

Girish Rayanagoudar

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Sabina Patel

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Susan Gelding

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P2860

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

Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia

Primary hypomagnesemia with secondary hypocalcemia in an infant.

The possible relationship between keratoconus and magnesium deficiency.

New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemia

Thalasselis syndrome and genetic theories on keratoconus.

Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: genetic linkage mapping and analysis of a balanced translocation breakpoint.

Influence of ethnic origin on the incidence of keratoconus and associated atopic disease in Asians and white patients.

P31

scholarly article

case report

P356

10.1136/BCR-2016-216870

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P478

2016

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P577

2016-09-13T00:00:00Z

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P698

27624449

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P932

5030594

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