FAM111A mutations result in hypoparathyroidism and impaired skeletal development

Unger, S (author)

Gorna, MW (author)

Le Bechec, A (author)

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Do Vale-Pereira, S (author)

Bedeschi, MF (author)

Geiberger, S (author)

Karolinska Institutet

Grigelioniene, G (author)

Karolinska Institutet

Horemuzova, E (author)

Karolinska Institutet

Lalatta, F (author)

Lausch, E (author)

Magnan, C (author)

Nampoothiri, S (author)

Nishimura, G (author)

Petrella, D (author)

Rojas-Ringeling, F (author)

Utsunomiya, A (author)

Zabel, B (author)

Pradervand, S (author)

Harshman, K (author)

Campos-Xavier, B (author)

Bonafe, L (author)

Superti-Furga, G (author)

Stevenson, B (author)

Superti-Furga, A (author)

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 (creator_code:org_t)

Elsevier BV, 2013

2013

English.

In: American journal of human genetics. - : Elsevier BV. - 1537-6605 .- 0002-9297. ; 92:6, s. 990-995

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• Journal article (peer-reviewed)