Neu-Laxova syndrome is a heterogeneous metabolic disorder caused by defects in enzymes of the L-serine biosynthesis pathway

Acuna-Hidalgo, R (author)

Schanze, D (author)

Kariminejad, A (author)

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Nordgren, A (author)

Karolinska Institutet

Kariminejad, MH (author)

Conner, P (author)

Grigelioniene, G (author)

Karolinska Institutet

Nilsson, D (author)

Karolinska Institutet

Nordenskjold, M (author)

Karolinska Institutet

Wedell, A (author)

Karolinska Institutet

Freyer, C (author)

Wredenberg, A (author)

Wieczorek, D (author)

Gillessen-Kaesbach, G (author)

Kayserili, H (author)

Elcioglu, N (author)

Ghaderi-Sohi, S (author)

Goodarzi, P (author)

Setayesh, H (author)

van de Vorst, M (author)

Steehouwer, M (author)

Pfundt, R (author)

Krabichler, B (author)

Curry, C (author)

MacKenzie, MG (author)

Boycott, KM (author)

Gilissen, C (author)

Janecke, AR (author)

Hoischen, A (author)

Zenker, M (author)

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 (creator_code:org_t)

Elsevier BV, 2014

2014

English.

In: American journal of human genetics. - : Elsevier BV. - 1537-6605 .- 0002-9297. ; 95:3, s. 285-293

Related links:

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• Journal article (peer-reviewed)