X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase a subunit

I.E.T. van den Berg; E.A.C.M. van Beurden; J.K. Ploos van Amstel

X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase a subunit

Translated title of the contribution: X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase a subunit

I.E.T. van den Berg
, E.A.C.M. van Beurden
, J.K. Ploos van Amstel

Department of Genetics

Research output: Contribution to journal › Article › Academic › peer-review

Translated title of the contribution	X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase a subunit
Original language	Undefined/Unknown
Pages (from-to)	381-387
Number of pages	7
Journal	American Journal of Human Genetics
Volume	56
Publication status	Published - 1995

Keywords

Econometric and Statistical Methods: General
Genetics
Geneeskunde(GENK)
Algemeen onderzoek

Cite this

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title = "X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase a subunit",

keywords = "Econometric and Statistical Methods: General, Genetics, Geneeskunde(GENK), Algemeen onderzoek",

author = "\{van den Berg\}, I.E.T. and \{van Beurden\}, E.A.C.M. and \{Ploos van Amstel\}, J.K.",

note = "keypublication",

year = "1995",

language = "Undefined/Unknown",

volume = "56",

pages = "381--387",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

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TY - JOUR

T1 - X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase a subunit

AU - van den Berg, I.E.T.

AU - van Beurden, E.A.C.M.

AU - Ploos van Amstel, J.K.

N1 - keypublication

PY - 1995

Y1 - 1995

KW - Econometric and Statistical Methods: General

KW - Genetics

KW - Geneeskunde(GENK)

KW - Algemeen onderzoek

M3 - Article

SN - 0002-9297

VL - 56

SP - 381

EP - 387

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

ER -